US5985558A - Antisense oligonucleotide compositions and methods for the inibition of c-Jun and c-Fos - Google Patents
Antisense oligonucleotide compositions and methods for the inibition of c-Jun and c-Fos Download PDFInfo
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- US5985558A US5985558A US08/837,201 US83720197A US5985558A US 5985558 A US5985558 A US 5985558A US 83720197 A US83720197 A US 83720197A US 5985558 A US5985558 A US 5985558A
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- oligonucleotide
- antisense oligonucleotide
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Classifications
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- C12N15/00—Mutation or genetic engineering; DNA or RNA concerning genetic engineering, vectors, e.g. plasmids, or their isolation, preparation or purification; Use of hosts therefor
- C12N15/09—Recombinant DNA-technology
- C12N15/11—DNA or RNA fragments; Modified forms thereof; Non-coding nucleic acids having a biological activity
- C12N15/113—Non-coding nucleic acids modulating the expression of genes, e.g. antisense oligonucleotides; Antisense DNA or RNA; Triplex- forming oligonucleotides; Catalytic nucleic acids, e.g. ribozymes; Nucleic acids used in co-suppression or gene silencing
- C12N15/1135—Non-coding nucleic acids modulating the expression of genes, e.g. antisense oligonucleotides; Antisense DNA or RNA; Triplex- forming oligonucleotides; Catalytic nucleic acids, e.g. ribozymes; Nucleic acids used in co-suppression or gene silencing against oncogenes or tumor suppressor genes
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K38/00—Medicinal preparations containing peptides
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- C12N2310/00—Structure or type of the nucleic acid
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- C12N2310/315—Phosphorothioates
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- C12N2310/00—Structure or type of the nucleic acid
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- C12N2310/31—Chemical structure of the backbone
- C12N2310/318—Chemical structure of the backbone where the PO2 is completely replaced, e.g. MMI or formacetal
- C12N2310/3181—Peptide nucleic acid, PNA
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- C12N2310/00—Structure or type of the nucleic acid
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Definitions
- the present invention provides compositions and methods for modulating levels of the c-fos and c-jun genes, which encode the c-Fos and c-Jun subunits of AP-1, respectively.
- AP-1 or transcription factor activating protein 1
- AP-1 is a heterogenous mixture of heterodimers of several related protein subunits including, in addition to c-Fos and c-Jun, FosB, Fra-1, Fra-2, c-Jun, JunB, JunD, etc.
- FOS and JUN Families of Proteins, Angel and Herrlich, eds., CRC Press, Boca Raton, Fla., 1994 The FOS and JUN Families of Proteins, Angel and Herrlich, eds., CRC Press, Boca Raton, Fla., 1994).
- AP-1 has been implicated in abnormal cell proliferation and tumor formation, events that thus might be controlled by modulating the expression of c-fos and/or c-jun.
- the invention is further directed to therapeutic, diagnostic, and research based reagents and methods for evaluating and treating disease states or disorders which result from and/or respond positively to modulation of one or more AP-1 subunits.
- disease states and disorders include those involving the hyperproliferation of cells such as, e.g., a tumor (neoplasm) or malignant cancer.
- Inhibition of AP-1-mediated hyperproliferation of cells, and corresponding prophylactic, palliative and therapeutic effects result from treatment with the oligonucleotides of the invention.
- Transcription factors play a central role in the expression of specific genes upon stimulation by extracellular signals, thereby regulating a complex array of biological processes.
- AP-1 activating protein-1
- cytokines cytokines
- tumor promoters tumor promoters
- carcinogens cytokines
- oncogenes growth factors and cytokines exert their function by binding to specific cell surface receptors.
- Receptor occupancy triggers a signal transduction cascade to the nucleus.
- transcription factors such as AP-1 execute long term responses to the extracellular factors by modulating gene expression.
- Such changes in cellular gene expression lead to DNA synthesis, and eventually the formation of differentiated derivatives (Angel and Karin, Biochim. Biophys. Acta, 1991, 1072, 129).
- AP-1 denotes one member of a family of related heterodimeric transcription factor complexes found in eukaryotic cells or viruses.
- AP-1 specifically refers to the heterodimer formed of c-Fos and c-Jun (Angel and Herrlich, Chapter 1, and Schuermann, Chapter 2 in: The FOS and JUN Families of Proteins, Angel and Herrlich, eds., pp. 3-35, CRC Press, Boca Raton, Fla., 1994; Bohmann et al., Science, 1987, 238, 1386; Angel et al., Nature, 1988, 332, 166).
- MAP Mitogen-activated protein
- PKC protein kinase C
- MEK1 and MEK2 The phosphorylation of proteins plays a key role in the transduction of extracellular signals into the cell.
- Mitogen-activated protein (MAP) kinases enzymes which effect such phosphorylations are targets for the action of growth factors, hormones, and other agents involved in cellular metabolism, proliferation and differentiation (Cobb et al., J. Biol. Chem., 1995, 270, 14843).
- MAP kinases are themselves activated by phosphorylation catalyzed by, e.g., receptor tyrosine kinases, G protein-coupled receptors, protein kinase C (PKC), and the apparently MAP kinase dedicated kinases MEK1 and MEK2.
- MAP kinases include, but are not limited to, ERK1, ERK2, two isoforms of ERK3, ERK4 (ERK stands for "extracellular signal-regulated protein kinase), Jun N-terminal kinases/stress-activated protein kinases (JNKs/SAPKs), p38/HOG1, p57 MAP kinases, MKK3 (MAP kinase kinase 3) and MKK4 (MAP kinase kinase 4, also known as SAPK/ERK kinase (SEK) or JNK kinase (JNKK)) (Cobb et al., J. Biol.
- ERK extracellular signal-regulated protein kinase
- JNKs/SAPKs Jun N-terminal kinases/stress-activated protein kinases
- JNKs/SAPKs Jun N-terminal kinases/stress-activated protein kinases
- MAP kinases are involved in a variety of signal transduction pathways (sometimes overlapping and sometimes parallel) that function to convey extracellular stimuli to protooncogene products to modulate cellular proliferation and/or differentiation.
- One of the signal transduction pathways involves the MAP kinases Jun kinase 1 and Jun kinase 2 which are responsible for the phosphorylation of specific sites (Serine 63 and Serine 73) on c-Jun. Phosphorylation of these sites potentiates the ability of AP-1 to activate transcription (Binetruy et al., Nature, 1991, 351, 122; Smeal et al., Nature, 1991, 354, 494). At least one human leukemia oncogene has been shown to enhance Jun N-terminal Kinase (JNK) function (Raitano et al., Proc. Natl. Acad. Sci.
- JNK Jun N-terminal Kinase
- malignant tumors or cancers comprise cells that are capable of undergoing metastasis, i.e., a process by which hyperproliferative cells spread to, and secure themselves within, other parts of the body via the circulatory or lymphatic system (see, generally, Chapter 16 In: Molecular Biology of the Cell, Alberts et al., eds., pp. 891-950, Garland Publishing, Inc., New York, 1983).
- metastasis i.e., a process by which hyperproliferative cells spread to, and secure themselves within, other parts of the body via the circulatory or lymphatic system
- inhibition of expression of c-fos and/or c-jun serves as a means to modulate the metastasis of malignant tumors.
- a method of modulating one or more metastatic events using the oligonucleotides of the invention is thus herein provided.
- Soprano et al. (Ann. N. Y. Acad. Sci., 1992, 660, 231) have used antisense oligodeoxynucleotides targeted to c-jun mRNA to study their ability to inhibit DNA synthesis and cell division.
- Liu et al. (Ann. Neurol., 1994, 36, 566) describe the suppression of c-fos by intraventricular infusion of an antisense oligodeoxynucleotide targeted to c-fos mRNA.
- Gillardon et al. describe the topical application of c-fos antisense oligodeoxynucleotides to the rat spinal cord (Eur. J. Neurosci., 1994, 6, 880) ultraviolet (UV)-exposed rat eyes (British J. Ophthal., 1995, 79, 277) and UV-irradiated rat skin (Carcinogenesis, 1995, 16, 1853).
- U.S. Pat. No. 5,602,156 which issued Feb. 11, 1997, to Kohn et al., discloses non-oligonucleotide compositions and methods for inhibiting the expression of two metalloproteinases, MMP-1 and MMP-2.
- compositions and methods of the invention overcome these limitations. Further objectives of the invention are apparent from the present disclosure.
- oligonucleotides are provided which specifically hybridize with nucleic acids encoding c-Fos or c-Jun.
- Certain oligonucleotides of the invention are designed to bind either directly to mRNA transcribed from, or to a selected DNA portion of, the respective gene, thereby modulating the amount of protein translated from a c-fos or c-jun mRNA and/or the amount of mRNA transcribed from a c-fos or c-jun gene, respectively.
- Such modulation can, in turn, effect the modulation of enzymes and cellular processes involved in the metastasis of malignant cells.
- Oligonucleotides may comprise nucleotide sequences sufficient in identity and number to effect specific hybridization with a particular nucleic acid. Such oligonucleotides are commonly described as “antisense.” Antisense oligonucleotides are commonly used as research reagents, diagnostic aids, and therapeutic agents.
- c-fos and c-jun genes encoding the c-Fos and c-Jun proteins, respectively, are particularly amenable to this approach.
- modulation of the expression of c-fos and/or c-jun leads to modulation of AP-1, and, accordingly, modulation of cellular proliferation.
- Such modulation is desirable for treating or modulating various hyperproliferative disorders or diseases, such as various cancers.
- Such inhibition is further desirable for preventing or modulating the development of such diseases or disorders in an animal suspected of being, or known to be, prone to such diseases or disorders.
- modulation of one subunit can be combined with modulation of the subunit of AP-1 in order to achieve a requisite degree of effect upon AP-1-mediated transcription.
- Methods of modulating the expression of c-Fos or c-Jun proteins comprising contacting animals with oligonucleotides specifically hybridizable with a c-fos or c-jun gene, respectively, are herein provided. These methods are believed to be useful both therapeutically and diagnostically as a consequence of the association between AP-1 expression and cellular proliferation. These methods are also useful as tools, for example, in the detection and determination of the role of AP-1 protein expression in various cell functions and physiological processes and conditions, and for the diagnosis of conditions associated with such expression and activation.
- the present invention also comprises methods of inhibiting AP-1-mediated transcriptional activation using the oligonucleotides of the invention.
- Methods of treating conditions in which abnormal or excessive AP-1-mediated transcriptional activation and cellular proliferation occur are also provided.
- These methods employ the oligonucleotides; of the invention and are believed to be useful both therapeutically and as clinical research and diagnostic tools.
- the oligonucleotides of the present invention may also be used for research purposes.
- the specific hybridization exhibited by the oligonucleotides of the present invention may be used for assays, purifications, cellular product preparations and in other methodologies which may be appreciated by persons of ordinary skill in the art.
- Methods comprising contacting animals with oligonucleotides specifically hybridizable with nucleic acids encoding c-Fos or c-Jun proteins are herein provided. Such methods can be used to modulate or detect the expression of c-fos or c-jun genes and are thus believed to be useful both therapeutically and diagnostically.
- the methods disclosed herein are also useful, for example, as clinical research tools in the detection and determination of the role of AP-1-mediated gene expression in various immune system functions and physiological processes and conditions, and for the diagnosis of conditions associated with their expression.
- the specific hybridization exhibited by the oligonucleotides of the present invention may be used for assays, purifications, cellular product preparations and in other methodologies which may be appreciated by persons of ordinary skill in the art.
- the oligonucleotides of this invention specifically hybridize to nucleic acids encoding c-Fos or c-Jun, sandwich and other assays can easily be constructed to exploit this fact.
- Detection of specific hybridization of an oligonucleotide of the invention with a nucleic acid encoding a c-Fos or c-Jun protein present in a sample can routinely be accomplished. Such detection may include detectably labeling an oligonucleotide of the invention by enzyme conjugation, radiolabeling or any other suitable detection system.
- a number of assays may be formulated employing the present invention, which assays will commonly comprise contacting a tissue or cell sample with a detectably labeled oligonucleotide of the present invention under conditions selected to permit hybridization and measuring such hybridization by detection of the label, as is appreciated by those of ordinary skill in the art.
- the present invention employs oligonucleotides for use in antisense inhibition of the function of RNA and DNA encoding a c-Fos protein or a c-Jun protein.
- the present invention also employs oligonucleotides which are designed to be specifically hybridizable to DNA or messenger RNA (mRNA) encoding such proteins and ultimately modulating the amount of such proteins transcribed from their respective genes.
- mRNA messenger RNA
- mRNA to be interfered with include all vital functions such as translocation of the RNA to the site for protein translation, actual translation of protein from the RNA, splicing of the RNA to yield one or more mRNA species, and possibly even independent catalytic activity which may be engaged in by the RNA.
- the overall effect of such interference with mRNA function is modulation of the expression of a c-Fos protein or a c-Jun protein.
- modulation means either an increase (stimulation) or a decrease (inhibition) in the expression of a gene. In the context of the present invention, inhibition is the preferred form of modulation of gene expression.
- oligonucleotide refers to an oligomer or polymer of ribonucleic acid or deoxyribonucleic acid. This term includes oligonucleotides composed of naturally-occurring nucleobases, sugars and covalent intersugar (backbone) linkages as well as oligonucleotides having non-naturally-occurring portions which function similarly. Such modified or substituted oligonucleotides are often preferred over native forms because of desirable properties such as, for example, enhanced cellular uptake, enhanced binding to target and increased stability in the presence of nucleases.
- An oligonucleotide is a polymer of a repeating unit generically known as a nucleotide.
- An unmodified (naturally occurring) nucleotide has three components: (1) a nitrogenous base linked by one of its nitrogen atoms to (2) a 5-carbon cyclic sugar and (3) a phosphate, esterified to carbon 5 of the sugar.
- the phosphate of a first nucleotide is also esterified to carbon 3 of the sugar of a second, adjacent nucleotide.
- the "backbone” of an unmodified oligonucleotide consists of (2) and (3), that is, sugars linked together by phosphodiester linkages between the carbon 5 (5') position of the sugar of a first nucleotide and the carbon 3 (3') position of a second, adjacent nucleotide.
- a "nucleoside” is the combination of (1) a nucleobase and (2) a sugar in the absence of (3) a phosphate moiety (Kornberg, A., DNA Replication, pp. 4-7, W. H. Freeman & Co., San Francisco, 1980).
- the backbone of an oligonucleotide positions a series of bases in a specific order; the written representation of this series of bases, which is conventionally written in 5' to 3' order, is known as a nucleotide sequence.
- the oligonucleotides in accordance with this invention preferably comprise from about 8 to about 30 nucleotides. It is more preferred that such oligonucleotides comprise from about 15 to 25 nucleotides.
- Oligonucleotides may comprise nucleotide sequences sufficient in identity and number to effect specific hybridization with a particular nucleic acid. Such oligonucleotides which specifically hybridize to a portion of the sense strand of a gene are commonly described as "antisense.” Antisense oligonucleotides are commonly used as research reagents, diagnostic aids, and therapeutic agents. For example, antisense oligonucleotides, which are able to inhibit gene expression with 17, specificity, are often used by those of ordinary skill to elucidate the function of particular genes, for example to distinguish between the functions of various members of a biological pathway. This specific inhibitory effect has, therefore, been harnessed by those skilled in the art for research uses.
- oligonucleotides demonstrate palliative, therapeutic and other methods utilizing antisense oligonucleotides.
- U.S. Pat. No. 5,135,917 provides antisense oligonucleotides that inhibit human interleukin-1 receptor expression.
- U.S. Pat. No. 5,098,890 is directed to antisense oligonucleotides complementary to the c-myb oncogene and antisense oligonucleotide therapies for certain cancerous conditions.
- U.S. Pat. No. 5,166,195 provides oligonucleotide inhibitors of Human Immunodeficiency Virus (HIV).
- U.S. Pat. No. 5,004,810 provides oligomers capable of hybridizing to herpes simplex virus Vmw65 mRNA and inhibiting replication.
- U.S. Pat. No. 5,194,428 provides antisense oligonucleotides having antiviral activity against influenzavirus.
- U.S. Pat. No. 4,806,463 provides antisense oligonucleotides and methods using them to inhibit HTLV-III replication.
- 5,286,717 provides oligonucleotides having a complementary base sequence to a portion of an oncogene.
- U.S. Pat. No. 5,276,019 and U.S. Pat. No. 5,264,423 are directed to phosphorothioate oligonucleotide analogs used to prevent replication of foreign nucleic acids in cells.
- U.S. Pat. No. 4,689,320 is directed to antisense oligonucleotides as antiviral agents specific to cytomegalovirus (CMV).
- CMV cytomegalovirus
- U.S. Pat. No. 5,098,890 provides oligonucleotides complementary to at least a portion of the mRNA transcript of the human c-myb gene.
- U.S. Pat. No. 5,242,906 provides antisense oligonucleotides useful in the treatment of latent Epstein-Barr virus (EBV) infections.
- EBV Epstein-Barr virus
- Targeting an oligonucleotide to the associated nucleic acid, in the context of this invention, is a multistep process. The process usually begins with the identification of a nucleic acid sequence whose function is to be modulated. This may be, for example, a cellular gene (or mRNA transcribed from the gene) whose expression is associated with a particular disorder or disease state, or a foreign nucleic acid from an infectious agent.
- the target is a cellular gene (c-fos or c-jun) encoding a subunit of AP-1, for which modulation is desired in certain instances.
- the targeting process also includes determination of a region (or regions) within this gene for the oligonucleotide interaction to occur such that the desired effect, either detection or modulation of expression of the protein, will result. Once the target region have been identified, oligonucleotides are chosen which are sufficiently complementary to the target, i.e., hybridize sufficiently well and with sufficient specificity to give the desired effect.
- the region of the 5' Cap a specialized structure that at least partially mediates ribosome binding
- the 5' untranslated (noncoding) region hereinafter, the "5'-UTR”
- the translation initiation codon region hereinafter, the "tIR”
- the open reading frame hereinafter, the "ORF”
- the translation termination codon region hereinafter, the "tTR”
- the 3' untranslated (noncoding) region hereinafter, the "3'-UTR"
- these regions are arranged in a typical messenger RNA molecule in the following order (left to right, 5' to 3'): 5' Cap, 5'-UTR, tIR, ORF, tTR, 3'-UTR, poly A tail.
- ORFs contain one or more sequences, known as "introns,” which are excised from a transcript before it is translated; the expressed (unexcised) portions of the ORF are referred to as "exons" (Alberts et al., Molecular Biology of the Cell, pp. 331-332 and 411-415, Garland Publishing Inc., New York, 1983).
- an ORF contains one or more sites that may be targeted due to some functional significance in vivo. Examples of the latter types of sites include intragenic stem-loop structures (see, e.g., U.S. Pat. No. 5,512,438) and, in unprocessed mRNA molecules, intron/exon splice sites.
- intragenic site is the region encompassing the translation initiation codon of the open reading frame (ORF) of the gene.
- the translation initiation codon is typically 5'-AUG (in transcribed mRNA molecules; 5'-ATG in the corresponding DNA molecule), the translation initiation codon is also referred to as the "AUG codon,” the “start codon” or the “AUG start codon.”
- a minority of genes have a translation initiation codon having the RNA sequence 5'-GUG, 5'-UUG or 5'-CUG, and 5'-AUA, 5'-ACG and 5'-CUG have been shown to function in vivo.
- 5'-UUU functions as a translation initiation codon in vitro (Brigstock et al., Growth Factors, 1990, 4, 45; Gelbert et al., Somat. Cell. Mol. Genet., 1990, 16, 173; Gold and Stormo, Chapter 78 in: Escherichia coli and Salmonella typhimurium: Cellular and Molecular Biology, Vol. 2, p. 1303, Neidhardt et al., eds., American Society for Microbiology, Washington, D.C., 1987).
- translation initiation codon and “start codon” can encompass many codon sequences, even though the initiator amino acid in each instance is typically methionine (in eukaryotes) or formylmethionine (prokaryotes).
- eukaryotic and prokaryotic genes may have two or more alternative start codons, any one of which may be preferentially utilized for translation initiation in a particular cell type or tissue, or under a particular set of conditions, in order to generate related polypeptides having different amino terminal sequences (Markussen et al., Development, 1995, 121, 3723; Gao et al., Cancer Res., 1995, 55, 743; McDermott et al., Gene, 1992, 117, 193; Perri et al., J. Biol. Chem., 1991, 266, 12536; French et al., J.
- start codon and “translation initiation codon” refer to the codon or codons that are used in vivo to initiate translation of an mRNA molecule transcribed from a gene encoding a c-Fos or c-Jun protein, regardless of the sequence(s) of such codons.
- a translation termination codon (or "stop codon”) of a gene may have one of three sequences, i.e., 5'-UAA, 5'-UAG and 5'-UGA (the corresponding DNA sequences are 5'-TAA, 5'-TAG and 5'-TGA, respectively).
- start codon region and “translation initiation region” refer to a portion of such an mRNA or gene that encompasses from about 25 to about 50 contiguous nucleotides in either direction (i.e., 5' or 3') from a translation initiation codon.
- stop codon region and “translation termination region” refer to a portion of such an mRNA or gene that encompasses from about 25 to about 50 contiguous nucleotides in either direction (i.e., 5' or 3') from a translation termination codon.
- oligonucleotide includes oligonucleotides composed of naturally-occurring nucleobases, sugars and covalent intersugar (backbone) linkages as well as oligonucleotides having non-naturally-occurring portions which function similarly. Such modified or substituted oligonucleotides may be preferred over native forms because of desirable properties such as, for example, enhanced cellular uptake, enhanced binding to target and increased stability in the presence of nucleases.
- modified oligonucleotides envisioned for this invention include those containing phosphorothioates, phosphotriesters, methyl phosphonates, short chain alkyl or cycloalkyl intersugar linkages or short chain heteroatomic or heterocyclic intersugar linkages.
- oligonucleotides with phosphorothioates and those with CH 2 --NH--O--CH 2 , CH 2 --N(CH 3 )--O--CH 2 [known as a methylene(methylimino) or MMI backbone], CH 2 --O--N(CH 3 )--CH 2 , CH 2 --N(CH 3 )--N(CH 3 )--CH 2 and O--N(CH 3 )--CH 2 --CH 2 backbones, wherein the native phosphodiester backbone is represented as O--P--O--CH 2 ).
- oligonucleotides having morpholino backbone structures (Summerton and Weller, U.S. Pat.
- oligonucleotides with NR--C(*)--CH 2 --CH 2 , CH 2 --NR--C(*)--CH 2 , CH 2 --CH 2 --NR--C(*), C(*)--NR--CH 2 --CH 2 and CH 2 --C(*)--NR--CH 2 backbones, wherein "*” represents O or S (known as amide backbones; DeMesmaeker et al., WO 92/20823, published Nov. 26, 1992).
- the phosphodiester backbone of the oligonucleotide is replaced with a polyamide backbone, the nucleobases being bound directly or indirectly to the aza nitrogen atoms of the polyamide backbone (Nielsen et al., Science, 1991, 254, 1497; U.S. Pat. No. 5,539,082).
- oligonucleotides of the invention may additionally or alternatively include nucleobase modifications or substitutions.
- nucleobase modifications or substitutions include adenine (A), guanine (G), thymine (T), cytosine (C) and uracil (U).
- Modified nucleobases include nucleobases found only infrequently or transiently in natural nucleic acids, e.g., hypoxanthine, 6-methyladenine, 5-methylcytosine, 5-hydroxymethylcytosine (HMC), glycosyl HMC and gentiobiosyl HMC, as well synthetic nucleobases, e.g., 2-aminoadenine, 2-thiouracil, 2-thiothymine, 5-bromouracil, 5-hydroxymethyluracil, 8-azaguanine, 7-deazaguanine, N 6 (6-aminohexyl)adenine and 2,6-diaminopurine (Kornberg, A., DNA Replication, pp. 75-77, W. H. Freeman & Co., San Francisco, 1980; Gebeyehu, G., et al., Nucleic Acids Res., 1987, 15, 4513).
- nucleobases found only infrequently or transiently in natural
- oligonucleotides of the invention may additionally or alternatively comprise substitutions of the sugar portion of the individual nucleotides.
- oligonucleotides may also have sugar mimetics such as cyclobutyls in place of the pentofuranosyl group.
- modified oligonucleotides may contain one or more substituted sugar moieties comprising one of the following at the 2' position: OH, SH, SCH 3 , F, OCN, OCH 3 OCH 3 , OCH 3 O(CH 2 ) n CH 3 , O(CH 2 ) n NH 2 or O(CH 2 ) n CH 3 where n is from 1 to about 10; C 1 to C 10 lower alkyl, alkoxyalkoxy, substituted lower alkyl, alkaryl or aralkyl; Cl; Br; CN; CF 3 ; OCF 3 ; O-, S-, or N-alkyl; O-, S-, or N-alkenyl; SOCH 3 ; SO 2 CH 3 ; ONO 2 ; NO 2 ; N 3 ; NH 2 ; heterocycloalkyl; heterocycloalkaryl; aminoalkylamino; polyalkylamino; substituted silyl; an RNA cleaving group;
- a preferred modification, particularly for orally deliverable pharmaceutical compositions, is 2'-methoxyethoxy [2'--O--CH 2 CH 2 OCH 3 , also known as 2'--O--(2-methoxyethyl)] (Martin et al., Helv. Chim. Acta, 1995, 78, 486).
- Other preferred modifications include 2'-methoxy (2'--O--CH 3 ), 2'-propoxy (2'--OCH 2 CH 2 CH 3 ) and 2'-fluoro (2'---F).
- oligonucleotide Similar modifications may also be made at other positions on the oligonucleotide, particularly the 3' position of the sugar on the 3' terminal nucleotide and the 5' position of 5' terminal nucleotide.
- the 5' and 3' termini of an oligonucleotide may also be modified to serve as points of chemical conjugation of, e.g., lipophilic moieties (see immediately subsequent paragraph), intercalating agents (Kuyavin et al., WO 96/32496, published Oct. 17, 1996; Nguyen et al., U.S. Pat. No. 4,835,263, issued May 30, 1989) or hydroxyalkyl groups (Helene et al., WO 96/34008, published Oct. 31, 1996).
- effector group is a chemical moiety that is capable of carrying out a particular chemical or biological function.
- effector groups include, but are not limited to, an RNA cleaving group, a reporter group, an intercalator, a group for improving the pharmacokinetic properties of an oligonucleotide, or a group for improving the pharmacodynamic properties of an oligonucleotide and other substituents having similar properties.
- a variety of chemical linkers may be used to conjugate an effector group to an oligonucleotide of the invention.
- U.S. Pat. No. 5,578,718 to Cook et al. discloses methods of attaching an alkylthio linker, which may be further derivatized to include additional groups, to ribofuranosyl positions, nucleosidic base positions, or on internucleoside linkages. Additional methods of conjugating oligonucleotides to various effector groups are known in the art; see, e.g., Protocols for Oligonucleotide Conjugates (Methods in Molecular Biology, Volume 26) Agrawal, S., ed., Humana Press, Totowa, N.J., 1994.
- oligonucleotides of the invention involves chemically linking to the oligonucleotide one or more lipophilic moieties which enhance the cellular uptake of the oligonucleotide.
- lipophilic moieties may be linked to an oligonucleotide at several different positions on the oligonucleotide. Some preferred positions include the 3' position of the sugar of the 3' terminal nucleotide, the 5' position of the sugar of the 5' terminal nucleotide, and the 2' position of the sugar of any nucleotide.
- the N 6 position of a purine nucleobase may also be utilized to link a lipophilic moiety to an oligonucleotide of the invention (Gebeyehu et al., Nucleic Acids Res., 1987, 15, 4513).
- lipophilic moieties include but are not limited to a cholesteryl moiety (Letsinger et al., Proc. Natl. Acad. Sci. USA, 1989, 86, 6553), cholic acid (Manoharan et al., Bioorg. Med. Chem.
- a thioether e.g., hexyl-S-tritylthiol
- a thiocholesterol Olet al., Nucl.
- oligonucleotides comprising lipophilic moieties, and methods for preparing such oligonucleotides, are disclosed in U.S. Pat. No. 5,138,045, No. 5,218,105 and No. 5,459,255, the contents of which are hereby incorporated by reference.
- the oligonucleotides of the invention may additionally or alternatively be prepared to be delivered in a "prodrug" form.
- prodrug indicates a therapeutic agent that is prepared in an inactive form that is converted to an active form (i.e., drug) within the body or cells thereof by the action of endogenous enzymes or other chemicals and/or conditions.
- prodrug versions of the oligonucleotides of the invention are prepared as SATE [(S-acetyl-2-thioethyl) phosphate] derivatives according to the methods disclosed in WO 93/24510 to Gosselin et al., published Dec. 9, 1993.
- the present invention also includes oligonucleotides that are substantially chirally pure with regard to particular positions within the oligonucleotides.
- substantially chirally pure oligonucleotides include, but are not limited to, those having phosphorothioate linkages that are at least 75% Sp or Rp (Cook et al., U.S. Pat. No. 5,587,361, issued Dec. 24, 1996) and those having substantially chirally pure (Sp or Rp) alkylphosphonate, phosphoamidate or phosphotriester linkages (Cook, U.S. Pat. No. 5,212,295, issued May 18, 1993; Cook, U.S. Pat. No. 5,521,302, issued May 28, 1996).
- the present invention also includes oligonucleotides which are chimeric oligonucleotides.
- "Chimeric" oligonucleotides or “chimeras,” in the context of this invention, are oligonucleotides which contain two or more chemically distinct regions, each made up of at least one nucleotide. These oligonucleotides typically contain at least one region wherein the oligonucleotide is modified so as to confer upon the oligonucleotide increased resistance to nuclease degradation, increased cellular uptake, and/or increased binding affinity for the target nucleic acid.
- An additional region of the oligonucleotide may serve as a substrate for enzymes capable of cleaving RNA:DNA or RNA:RNA hybrids.
- RNase H is a cellular endonuclease which cleaves the RNA strand of an RNA:DNA duplex. Activation of RNase H, therefore, results in cleavage of the RNA target, thereby greatly enhancing the efficiency of antisense inhibition of gene expression. Cleavage of the RNA target can be routinely detected by gel electrophoresis and, if necessary, associated nucleic acid hybridization techniques known in the art.
- such “chimeras” may be “gapmers,” i.e., oligonucleotides in which a central portion (the "gap") of the oligonucleotide serves as a substrate for, e.g., RNase H, and the 5' and 3' portions (the “wings”) are modified in such a fashion so as to have greater affinity for the target RNA molecule but are unable to support nuclease activity (e.g., 2'-fluoro- or 2'-methoxyethoxy substituted).
- nuclease activity e.g., 2'-fluoro- or 2'-methoxyethoxy substituted
- chimeras include "wingmers,” that is, oligonucleotides in which the 5' portion of the oligonucleotide serves as a substrate for, e.g., RNase H, whereas the 3' portion is modified in such a fashion so as to have greater affinity for the target RNA molecule but is unable to support nuclease activity (e.g., 2'-fluoro- or 2'-methoxyethoxy substituted), or vice-versa.
- wingmers that is, oligonucleotides in which the 5' portion of the oligonucleotide serves as a substrate for, e.g., RNase H, whereas the 3' portion is modified in such a fashion so as to have greater affinity for the target RNA molecule but is unable to support nuclease activity (e.g., 2'-fluoro- or 2'-methoxyethoxy substituted), or vice-versa.
- nuclease activity e.g
- oligonucleotides used in accordance with this invention may be conveniently and routinely made through the well-known technique of solid phase synthesis.
- Equipment for such synthesis is sold by several vendors including, for example, Applied Biosystems (Foster City, Calif.). Any other means for such synthesis known in the art may additionally or alternatively be employed. It is also known to use similar techniques to prepare other oligonucleotides such as the phosphorothioates and alkylated derivatives.
- Teachings regarding the synthesis of particular modified oligonucleotides are hereby incorporated by reference from the following U.S. patents or pending patent applications, each of which is commonly assigned with this application: U.S. Pat. Nos.
- 5,578,718 drawn to nucleosides having alkylthio groups, wherein such groups may be used as linkers to other moieties, attached at any of a variety of positions of the nucleoside; and U.S. Pat. No. 5,587,361, drawn to oligonucleotides having phosphorothioate linkages of high chiral purity.
- oligonucleotides of the present invention can be utilized as therapeutic compounds, diagnostic tools and as research reagents and kits.
- the term "therapeutic uses" is intended to encompass prophylactic, palliative and curative uses wherein the oligonucleotides of the invention are contacted with animal cells either in vivo or ex vivo. When contacted with animal cells ex vivo, a therapeutic use includes incorporating such cells into an animal after treatment with one or more oligonucleotides of the invention.
- an animal suspected of having a disease or disorder which can be treated or prevented by modulating the expression or activity of a c-Fos or c-Jun protein is, for example, treated by administering oligonucleotides in accordance with this invention.
- the oligonucleotides of the invention can be utilized in pharmaceutical compositions by adding an effective amount of an oligonucleotide to a suitable pharmaceutically acceptable diluent or carrier.
- Workers in the field have identified antisense, triplex and other oligonucleotide compositions which are capable of modulating expression of genes implicated in viral, fungal and metabolic diseases.
- Antisense oligonucleotides have been safely administered to humans and several clinical trials are presently underway. It is thus established that oligonucleotides can be useful therapeutic instrumentalities that can be configured to be useful in treatment regimes for treatment of cells, tissues and animals, especially humans.
- the oligonucleotides of the present invention can be further used to detect the presence of c-fos- or c-jun-specific nucleic acids in a cell or tissue sample.
- radiolabeled oligonucleotides can be prepared by 32 p labeling at the 5' end with polynucleotide kinase (Sambrook et al., Molecular Cloning. A Laboratory Manual, Vol. 2, p. 10.59, Cold Spring Harbor Laboratory Press, 1989).
- Radiolabeled oligonucleotides are then contacted with cell or tissue samples suspected of containing c-fos or c-jun message RNAs (and thus c-Fos or c-Jun proteins), and the samples are washed to remove unbound oligonucleotide. Radioactivity remaining in the sample indicates the presence of bound oligonucleotide, which in turn indicates the presence of nucleic acids complementary to the oligonucleotide, and can be quantitated using a scintillation counter or other routine means. Expression of nucleic acids encoding these proteins is thus detected.
- Radiolabeled oligonucleotides of the present invention can also be used to perform autoradiography of tissues to determine the localization, distribution and quantitation of c-Fos or c-Jun proteins for research, diagnostic or therapeutic purposes.
- tissue sections are treated with radiolabeled oligonucleotide and washed as described above, then exposed to photographic emulsion according to routine autoradiography procedures.
- the emulsion when developed, yields an image of silver grains over the regions expressing a c-Fos or c-Jun gene. Quantitation of the silver grains permits detection of the expression of mRNA molecules encoding these proteins and permits targeting of oligonucleotides to these areas.
- Analogous assays for fluorescent detection of expression of c-fos or c-jun nucleic acids can be developed using oligonucleotides of the present invention which are conjugated with fluorescein or other fluorescent tags instead of radiolabeling. Such conjugations are routinely accomplished during solid phase synthesis using fluorescently-labeled amidites or controlled pore glass (CPG) columns. Fluorescein-labeled amidites and CPG are available from, e.g., Glen Research (Sterling, Va.).
- kits for detecting the presence or absence of expression of a c-Fos and/or c-Jun protein may also be prepared.
- kits include an oligonucleotide targeted to an appropriate gene, i.e., a gene encoding a c-Fos or c-Jun protein.
- Hybridization of the oligonucleotides of the invention with a nucleic acid encoding a c-Fos or c-Jun protein can be detected by means known in the art. Such means may include conjugation of an enzyme to the oligonucleotide, radiolabelling of the oligonucleotide or any other suitable detection systems. Kits for detecting the presence or absence of a c-Fos or c-Jun protein may also be prepared.
- hybridization means hydrogen bonding, which may be Watson-Crick, Hoogsteen or reversed Hoogsteen hydrogen bonding, between complementary nucleotides.
- adenine and thymine are complementary nucleobases which pair through the formation of hydrogen bonds.
- “Complementary,” as used herein, refers to the capacity for precise pairing between two nucleotides. For example, if a nucleotide at a certain position of an oligonucleotide is capable of hydrogen bonding with a nucleotide at the same position of a DNA or RNA molecule, then the oligonucleotide and the DNA or RNA are considered to be complementary to each other at that position.
- oligonucleotide and the DNA or RNA are complementary to each other when a sufficient number of corresponding positions in each molecule are occupied by nucleotides which can hydrogen bond with each other.
- “specifically hybridizable” and “complementary” are terms which are used to indicate a sufficient degree of complementarity or precise pairing such that stable and specific binding occurs between the oligonucleotide and the DNA or RNA target. It is understood in the art that an oligonucleotide need not be 100% complementary to its target DNA sequence to be specifically hybridizable.
- An oligonucleotide is specifically hybridizable when binding of the oligonucleotide to the target DNA or RNA molecule interferes with the normal function of the target DNA or RNA to cause a decrease or loss of function, and there is a sufficient degree of complementarity to avoid non-specific binding of the oligonucleotide to non-target sequences under conditions in which specific binding is desired, i.e., under physiological conditions in the case of in vivo assays or therapeutic treatment, or in the case of in vitro assays, under conditions in which the assays are performed.
- oligonucleotide in accordance with the invention commonly in a pharmaceutically acceptable carrier, in doses ranging from 0.01 ug to 100 g per kg of body weight depending on the age of the patient and the severity of the disorder or disease state being treated.
- the treatment regimen may last for a period of time which will vary depending upon the nature of the particular disease or disorder, its severity and the overall condition of the patient, and may extend from once daily to once every 20 years. Following treatment, the patient is monitored for changes in his/her condition and for alleviation of the symptoms of the disorder or disease state.
- the dosage of the oligonucleotide may either be increased in the event the patient does not respond significantly to current dosage levels, or the dose may be decreased if an alleviation of the symptoms of the disorder or disease state is observed, or if the disorder or disease state has been abated.
- treatment regimen is meant to encompass therapeutic, palliative and prophylactic modalities.
- a patient may be treated with conventional chemotherapeutic agents, particularly those used for tumor and cancer treatment.
- chemotherapeutic agents include but are not limited to daunorubicin, daunomycin, dactinomycin, doxorubicin, epirubicin, idarubicin, esorubicin, bleomycin, mafosfamide, ifosfamide, cytosine arabinoside, bis-chloroethylnitrosurea, busulfan, mitomycin C, actinomycin D, mithramycin, prednisone, hydroxyprogesterone, testosterone, tamoxifen, dacarbazine, procarbazine, hexamethylmelamine, pentamethylmelamine, mitoxantrone, amsacrine, chlorambucil, methylcyclohexylnitrosurea, nitrogen mustards, melphalan, cyclophosphamide, 6-mercaptopurine, 6-thioguanine, cytarabine (CA), 5-azacytidine, hydroxyure
- chemotherapeutic agents may be used individually (e.g., 5-FU and oligonucleotide), sequentially (e.g., 5-FU and oligonucleotide for a period of time followed by MTX and oligonucleotide), or in combination with one or more other such chemotherapeutic agents (e.g., 5-FU, MTX and oligonucleotide, or 5-FU, radiotherapy and oligonucleotide).
- 5-FU and oligonucleotide e.g., 5-FU and oligonucleotide
- sequentially e.g., 5-FU and oligonucleotide for a period of time followed by MTX and oligonucleotide
- one or more other such chemotherapeutic agents e.g., 5-FU, MTX and oligonucleotide, or 5-FU, radiotherapy and oligonucleotide.
- a first antisense oligonucleotide targeted to c-fos is used in combination with a second antisense oligonucleotide targeted to c-jun in order to modulate AP-1 molecules to a more extensive degree than can be achieved when either oligonucleotide used individually.
- oligonucleotide is administered in maintenance doses, ranging from 0.01 ug to 100 g per kg of body weight, once or more daily, to once every 20 years.
- prophylactic effects may be achieved by administration of preventative doses, ranging from 0.01 ug to 100 g per kg of body weight, once or more daily, to once every 20 years.
- compositions of the present invention may be administered in a number of ways depending upon whether local or systemic treatment is desired and upon the area to be treated.
- administration indicates the topical (including ophthalmic, vaginal, rectal, intranasal, transdermal), oral or parenteral contacting of an oligonucleotide, or pharmaceutical composition comprising an oligonucleotide, with cells, tissues or organs of a mammal including a human.
- Parenteral administration includes intravenous drip; subcutaneous, intraperitoneal, intravitreal or intramuscular injection; and intrathecal or intraventricular administration as herein described.
- Formulations for topical administration may include transdermal patches, ointments, lotions, creams, gels, drops, suppositories, sprays, liquids and powders.
- Conventional pharmaceutical carriers, nucleic acid carriers, aqueous, powder or oily bases, thickeners and the like may be necessary or desirable in certain instances.
- Topical administration also includes the delivery of oligonucleotides into the epidermis of a mammal by electroporation (Zewert et al., WO 96/39531, published Dec. 12, 1996).
- compositions for oral administration include powders or granules, suspensions or solutions in water or non-aqueous media, capsules, sachets or tablets. Thickeners, flavoring agents, diluents, emulsifiers, dispersing aids or binders may be desirable.
- Intravitreal injection for the direct delivery of drug to the vitreous humor of a mammalian eye, is described in U.S. Pat. No. 5,595,978, which issued Jan. 21, 1997, and which is assigned to the same assignee as the instant application, the contents of which are hereby incorporated by reference.
- Intraluminal drug administration for the direct delivery of drug to an isolated portion of a tubular organ or tissue (e.g., such as an artery, vein, ureter or urethra), may be desired for the treatment of patients with diseases or conditions afflicting the lumen of such organs or tissues.
- a catheter or cannula is surgically introduced by appropriate means.
- a cannula is inserted thereinto via the external carotid artery.
- a composition comprising the oligonucleotides of the invention is infused through the cannula or catheter into the isolated segment.
- the infusion cannula or catheter is removed and flow within the tubular organ or tissue is restored by removal of the ligatures which effected the isolation of a segment thereof (Morishita et al., Proc. Natl. Acad. Sci. (U.S.A.), 1993, 90, 8474).
- Antisense oligonucleotides may also be combined with a biocompatible matrix or carrier, such as a hydrogel material, and applied directly to vascular tissue in vivo (Rosenberg et al., U.S. Pat. No. 5,593,974, issued Jan. 14, 1997).
- a biocompatible matrix or carrier such as a hydrogel material
- Intraventricular drug administration for the direct delivery of drug to the brain of a patient, may be desired for the treatment of patients with diseases or conditions afflicting the brain.
- a silicon catheter is surgically introduced into a ventricle of the brain of a human patient, and is connected to a subcutaneous infusion pump (Medtronic Inc., Minneapolis, Minn.) that has been surgically implanted in the abdominal region (Zimm et al., Cancer Research, 1984, 44, 1698; Shaw, Cancer, 1993, 72(11 Suppl.), 3416).
- the pump is used to inject the oligonucleotides and allows precise dosage adjustments and variation in dosage schedules with the aid of an external programming device.
- the reservoir capacity of the pump is 18-20 mL and infusion rates may range from 0.1 mL/h to 1 mL/h.
- the pump reservoir may be refilled at 3-10 week intervals. Refilling of the pump is accomplished by percutaneous puncture of the self-sealing septum of the pump.
- Intrathecal drug administration for the introduction of drug into the spinal column of a patient may be desired for the treatment of patients with diseases of the central nervous system.
- a silicon catheter is surgically implanted into the L3-4 lumbar spinal interspace of a human patient, and is connected to a subcutaneous infusion pump which has been surgically implanted in the upper abdominal region (Luer and Hatton, The Annals of Pharmacotherapy, 1993, 27, 912; Ettinger et al., 1978, Cancer, 41, 1270, 1978; Yaida et al., Regul. Pept., 1995, 59, 193).
- the pump is used to inject the oligonucleotides and allows precise dosage adjustments and variations in dose schedules with the aid of an external programming device.
- the reservoir capacity of the pump is 18-20 mL, and infusion rates may vary from 0.1 mL/h to 1 mL/h.
- the pump reservoir may be refilled at 3-10 week intervals. Refilling of the pump is accomplished by a single percutaneous puncture to the self-sealing septum of the pump.
- the distribution, stability and pharmacokinetics of oligonucleotides within the central nervous system may be followed according to known methods (Whitesell et al., Proc. Natl. Acad. Sci (USA), 1993, 90, 4665).
- the silicon catheter is configured to connect the subcutaneous infusion pump to, e.g., the hepatic artery, for delivery to the liver (Kemeny et al., Cancer, 1993, 71:1964).
- Infusion pumps may also be used to effect systemic delivery of oligonucleotides (Ewel et al., Cancer Research, 1992, 52:3005; Rubenstein et al., J. Surg. Oncol., 1996, 62:194).
- colloidal dispersion systems may be used as delivery vehicles to enhance the in vivo stability of the oligonucleotides and/or to target the oligonucleotides to a particular organ, tissue or cell type.
- Colloidal dispersion systems include, but are not limited to, macromolecule complexes, nanocapsules, microspheres, beads and lipid-based systems including oil-in-water emulsions, micelles, mixed micelles and liposomes.
- a preferred colloidal dispersion system is a plurality of liposomes, artificial membrane vesicles which may be used as cellular delivery vehicles for bioactive agents in vitro and in vivo (Mannino et al., Biotechniques, 1988, 6, 682; Blume and Cevc, Biochem. et Biophys. Acta, 1990, 1029, 91; Lappalainen et al., Antiviral Res., 1994, 23, 119; Chonn and Cullis, Current Op. Biotech., 1995, 6, 698).
- RNA, DNA and intact virions can be encapsulated within the aqueous interior and delivered to brain cells in a biologically active form (Fraley et al., Trends Biochem. Sci., 1981, 6, 77).
- the composition of the liposome is usually a combination of lipids, particularly phospholipids, in particular, high phase transition temperature phospholipids, usually in combination with one or more steroids, particularly cholesterol.
- lipids useful in liposome production include phosphatidyl compounds, such as phosphatidylglycerol, phosphatidylcholine, phosphatidylserine, phosphatidylethanolamine, sphingolipids, cerebrosides and gangliosides. Particularly useful are diacyl phosphatidylglycerols, where the lipid moiety contains from 14-18 carbon atoms, particularly from 16-18 carbon atoms, and is saturated (lacking double bonds within the 14-18 carbon atom chain).
- Illustrative phospholipids include phosphatidylcholine, dipalmitoylphosphatidylcholine and distearoylphosphatidylcholine.
- the targeting of colloidal dispersion systems can be either passive or active. Passive targeting utilizes the natural tendency of liposomes to distribute to cells of the reticuloendothelial system in organs that contain sinusoidal capillaries. Active targeting, by contrast, involves modification of the liposome by coupling thereto a specific ligand such as a viral protein coat (Morishita et al., Proc. Natl. Acad. Sci.
- lipid groups can be incorporated into the lipid bilayer of the liposome in order to maintain the targeting ligand in close association with the lipid bilayer.
- Various linking groups can be used for joining the lipid chains to the targeting ligand.
- the targeting ligand which binds a specific cell surface molecule found predominantly on cells to which delivery of the oligonucleotides of the invention is desired, may be, for example, (1) a hormone, growth factor or a suitable oligopeptide fragment thereof which is bound by a specific cellular receptor predominantly expressed by cells to which delivery is desired or (2) a polyclonal or monoclonal antibody, or a suitable fragment thereof (e.g., Fab; F(ab') 2 ) which specifically binds an antigenic epitope found predominantly on targeted cells.
- Two or more bioactive agents e.g., an oligonucleotide and a conventional drug; two oligonucleotides
- colloidal dispersion systems which enhance the intercellular stability and/or targeting of the contents thereof.
- compositions for parenteral, intrathecal or intraventricular administration, or colloidal dispersion systems may include sterile aqueous solutions which may also contain buffers, diluents and other suitable additives. Dosing is dependent on severity and responsiveness of the disease state to be treated, with the course of treatment lasting from several days to several months, or until a cure is effected or a diminution of the disease state is achieved. Optimal dosing schedules can be calculated from measurements of drug accumulation in the body of the patient. Persons of ordinary skill can easily determine optimum dosages, dosing methodologies and repetition rates.
- Optimum dosages may vary depending on the relative potency of individual oligonucleotides, and can generally be estimated based on EC 50 s found to be effective in in vitro and in vivo animal models. In general, dosage is from 0.01 ⁇ g to 100 g per kg of body weight, and may be given once or more daily, weekly, monthly or yearly, or even once every 2 to 20 years.
- Oligonucleotides were synthesized on an automated DNA synthesizer using standard phosphoramidite chemistry with oxidation using iodine. ⁇ -Cyanoethyldiisopropyl phosphoramidites were purchased from Applied Biosystems (Foster City, Calif.). For phosphorothioate oligonucleotides, the standard oxidation bottle was replaced by a 0.2 M solution of 3H-1,2-benzodithiole-3-one-1,1-dioxide in acetonitrile for the stepwise thiation of the phosphite linkages.
- the 2'-fluoro-phosphorothioate oligonucleotides of the invention were synthesized using 5'-dimethoxytrityl-3'-phosphoramidites and prepared as disclosed in U.S. patent application Ser. No. 08/383,666, filed Feb. 3, 1995, and U.S. Pat. No. 5,459,255, which issued Oct. 8, 1996, both of which are assigned to the same assignee as the instant application and which are incorporated by reference herein.
- the 2'-fluoro-oligonucleotides were prepared using phosphoramidite chemistry and a slight modification of the standard DNA synthesis protocol (i.e., deprotection was effected using methanolic ammonia at room temperature).
- the 2'-methoxyethoxy oligonucleotides were synthesized essentially according to the methods of Martin et al. (Helv. Chim. Acta, 1995, 78, 486).
- the 3' nucleotide of the 2'-methoxyethoxy oligonucleotides was a deoxynucleotide, and 2'-O--CH 2 CH 2 OCH 3- cytosines were 5-methyl cytosines, which were synthesized according to the procedures described below.
- PNA antisense analogs were prepared essentially as described in U.S. Pat. Nos. 5,539,082 and 5,539,083, both of which (1) issued Jul. 23, 1996, (2) are assigned to the same assignee as the instant application and (3) are incorporated by reference herein.
- Oligonucleotides comprising 2,6-diaminopurine were prepared essentially as described in U.S. Pat. No. 5,506,351 which issued Apr. 9, 1996, is assigned to the same assignee as the instant application and which is incorporated by reference herein. Oligonucleotides comprising 2,6-diaminopurine can also be prepared by enzymatic means (Bailly et al., Proc. Natl. Acad. Sci. U.S.A., 1996, 93:13623).
- oligonucleotides were purified by precipitation 2 ⁇ from 0.5 M NaCl with 2.5 volumes of ethanol. Analytical gel electrophoresis was accomplished in 20% acrylamide, 8 M urea and 45 mM Tris-borate buffer (pH 7).
- 5-Methyluridine (ribosylthymine, commercially available through Yamasa, Choshi, Japan) (72.0 g, 0.279 M), diphenylcarbonate (90.0 g, 0.420 M) and sodium bicarbonate (2.0 g, 0.024 M) were added to DMF (300 mL). The mixture was heated to reflux, with stirring, allowing the evolved carbon dioxide gas to be released in a controlled manner. After 1 hour, the slightly darkened solution was concentrated under reduced pressure. The resulting syrup was poured into diethylether (2.5 L), with stirring. The product formed a gum. The ether was decanted and the residue was dissolved in a minimum amount of methanol (ca. 400 mL).
- the solution was poured into fresh ether (2.5 L) to yield a stiff gum.
- the ether was decanted and the gum was dried in a vacuum oven (60° C. at 1 mm Hg for 24 h) to give a solid which was crushed to a light tan powder (57 g, 85% crude yield). The material was used as is for further reactions.
- 2,2'-Anhydro-5-methyluridine (195 g, 0.81 M), tris(2-methoxyethyl)borate (231 g, 0.98 M) and 2-methoxyethanol (1.2 L) were added to a 2 L stainless steel pressure vessel and placed in a preheated oil bath at 160° C. After heating for 48 hours at 155-160° C., the vessel was opened and the solution evaporated to dryness and triturated with MeOH (200 mL). The residue was suspended in hot acetone (1 L). The insoluble salts were filtered, washed with acetone (150 mL) and the filtrate evaporated. The residue (280 g) was dissolved in CH 3 CN (600 mL) and evaporated.
- a first solution was prepared by dissolving 3'-O-acetyl-2'-O-methoxyethyl-5'-O-dimethoxytrityl-5-methyluridine (96 g, 0.144 M) in CH 3 CN (700 mL) and set aside. Triethylamine (189 mL, 1.44 M) was added to a solution of triazole (90 g, 1.3 M) in CH 3 CN (1 L), cooled to -5° C. and stirred for 0.5 h using an overhead stirrer. POCl 3 was added dropwise, over a 30 minute period, to the stirred solution maintained at 0-10° C., and the resulting mixture stirred for an additional 2 hours.
- the first solution was added dropwise, over a 45 minute period, to the later solution.
- the resulting reaction mixture was stored overnight in a cold room. Salts were filtered from the reaction mixture and the solution was evaporated. The residue was dissolved in EtOAc (1 L) and the insoluble solids were removed by filtration. The filtrate was washed with 1 ⁇ 300 mL of NaHCO 3 and 2 ⁇ 300 mL of saturated NaCl, dried over sodium sulfate and evaporated. The residue was triturated with EtOAc to give the title compound.
- Table 1 shows the sequence and activity of each of the oligonucleotides evaluated for inhibition of c-jun mRNA expression
- Table 2 shows the sequence and activity of the oligonucleotides evaluated for inhibition of c-fos mRNA expression.
- Oligonucleotide activities were evaluated as described infra in Example 2 et seq.
- For the nucleotide sequence of the human c-jun gene see Hattori et al., Proc. Natl. Acad. Sci. U.S.A., 1988, 85:9148, and Genbank accession No. J04111 ("HUMJUNA").
- the nucleotide sequence of the human c-fos gene is described by Van Straaten et al., Proc. Natl. Acad. Sci. U.S.A., 1983, 80:3183, and in Genbank accession No. K00650 ("HUMFOS").
- A549 cells were grown in T-75 flasks until 80-90% confluent.
- Cell line A549 is available from, inter alia, the American Type Culture Collection, Rockville, Md., as ATCC No.
- the cells were washed twice with 10 mL of media (DMEM), followed by the addition of 5 mL of DMEM containing 20 ⁇ g/mL of LIPOFECTINTM (i.e., DOTMA/DOPE (N-[1-(2,3-dioleyloxy)propyl]-N,N,N-triethylammonium chloride/dioleoylphosphatidyl ethanolamine)).
- LIPOFECTINTM i.e., DOTMA/DOPE (N-[1-(2,3-dioleyloxy)propyl]-N,N,N-triethylammonium chloride/dioleoylphosphatidyl ethanolamine
- DOTMA/DOPE N-[1-(2,3-dioleyloxy)propyl]-N,N,N-triethylammonium chloride/dioleoylphosphatidyl ethanolamine
- ISIS 10580, 10581, 10582 and 10583 were most active (81%, 76%, 83% and 80% inhibition, respectively).
- Treatment of cells with these oligonucleotides reduced c-jun expression to 19%, 24%, 17% and 20% (81%, 76%, 83% and 80% inhibition), respectively, of the level seen in control experiments (100% expression, 0% inhibition).
- Basal levels of c-jun mRNA are typically about 30% of the control value; ISIS 10572, 10578 and 10579 reduce c-jun levels to near basal levels (39%, 37% and 41%, respectively) and are thus also preferred.
- the oligonucleotides most effective in reducing c-fos mRNA expression are ISIS 10633, 10635, 10638 and 10639. Treatment of cells with these oligonucleotides reduced c-fos expression to 24%, 12%, 22% and 9% (76%, 88%, 78% and 91% inhibition), respectively, of the level seen in control experiments (100% expression, 0% inhibition); basal levels of c-fos mRNA are typically about 3% of the control value. These oligonucleotides effect significant inhibition of c-fos and are therefor preferred.
- oligonucleotide-mediated inhibition of c-fos and c-jun mRNA expression was further examined by determining the effects of scrambled, 6- or 7-base mismatch and sense control versions of the most active oligonucleotides, ISIS 10582 (c-jun) and ISIS 10639 (c-fos).
- ISIS 10582 exhibited potent and specific inhibition of c-jun mRNA expression, but ISIS 11562 (sense version of ISIS 10582; SEQ ID NO:29), ISIS 11564 (6 base pair mismatch version of ISIS 10639; SEQ ID NO:31) and ISIS 11563 (scrambled version of ISIS 10639; SEQ ID NO:30) had no detectable effect on c-jun mRNA levels during TPA induction (the sequences of ISIS 11562-11564 are given in Table 1).
- ISIS 10639 exhibited potent and specific inhibition of c-fos mRNA expression, but ISIS 11184 (sense version of ISIS 10639; SEQ ID NO:32), ISIS 11185 (7 base pair mismatch version of ISIS 10639; SEQ ID NO:33) and ISIS 11186 (scrambled version of ISIS 10639; SEQ ID NO:34) had no detectable effect on c-fos mRNA levels during TPA induction (the sequences of ISIS 11184-11186 are given in Table 2).
- neither active oligonucleotide has any detectable effect on mRNA levels of the other active oligonucleotide's target. That is, ISIS 10639, targeted to c-fos, has no detectable effect on c-jun levels; similarly, ISIS 10582, targeted to c-jun, has no detectable effect on c-fos levels.
- ISIS 10582 effects potent and specific modulation (i.e., inhibition) of c-jun mRNA levels and that ISIS 10639 effects potent and specific modulation of c-fos mRNA levels.
- c-fos active oligonucleotide ISIS 10639 was examined as follows. A549 cells were treated with oligonucleotides as in Examples 2-3, except that induction of c-Fos was effected by treatment of cells with TPA (1 uM) for three hours. At this time, whole cell protein was extracted in SDS (sodium dodecyl sulfate) buffer. Samples of extracts were electrophoresed, transferred to nitrocellulose filters which were immunoblotted using a c-Fos-specific antibody (Santa Cruz AB, Santa Cruz, Calif.). The results (Table 7) demonstrate that treatment of cells with the c-fos antisense oligonucleotide results in basal levels of c-Fos protein.
- SDS sodium dodecyl sulfate
- oligonucleotides that modulate c-Fos or c-Jun are identified, derivative or modified oligonucleotides having the same sequence thereas are prepared.
- the modified oligonucleotides described in Tables 8 and 9 were prepared.
- the effect of the c-fos-targeted oligonucleotides on c-fos RNA levels were evaluated as described in Examples 2-3.
- the results (Table 10) demonstrate that some enhancement of c-fos modulation can be achieved by the use modifications such as, e.g., 2'-fluoro (ISIS 11200).
- PNA analogs of the invention are introduced into appropriate cell lines by microinjection according to the method of Hanvey et al. (Science, 1992, 258:1481). Intracellular delivery of PNA analogs is confirmed by the use of a fluorescently tagged PNA antisense analog conjugate such as, e.g., ISIS 14240.
- Tables 11 and 12 show the sequences of oligonucleotides designed to modulate mouse c-jun and c-fos mRNA expression, respectively.
- nucleotide sequence of the mouse c-jun gene see Genbank accession No. J04115/MUSCJUN and Ryder et al., Proc. Natl. Acad. Sci. U.S.A., 1988, 85:8464.
- the nucleotide sequence of the mouse c-fos gene is described in Genbank accession No. J00370/MUSFOS and by Van Beveren et al., Cell, 1983, 32:1241. Oligonucleotide activities are evaluated as described infra in Example 2 et seq.
- mouse Swiss 3T3 cells available from, inter alia, the American Type Culture Collection, Rockville, Md., as ATCC No. CCL-92
- human A549 cells Due to the high degree of homology between human and murine c-jun and c-fos nucleotide sequences (Van Straaten et al., Proc. Natl. Acad. Sci. U.S.A., 1983, 80:3183), probes derived from the human genes were used to detect murine messages.
- Tables 13 and 14 show the sequences of oligonucleotides designed to modulate rat c-jun and c-fos mRNA expression, respectively.
- nucleotide sequence of the rat c-jun gene see Genbank accession No. X17163/RSJUNAP1 and Saaki et al., Cancer Res., 1989, 49:5633.
- the nucleotide sequence of the rat c-fos gene is described in Genbank accession No. X06769/RNCFOSR and Curran et al., Oncogene, 1987, 2:79. Oligonucleotide activities were evaluated as described infra in Example 2 et seq.
- rat A10 cells available from, inter alia, the American Type Culture Collection, Rockville, Md., as ATCC No. CRL-1476
- human A549 cells Due to the high degree of homology between human and rat c-jun and c-fos nucleotide sequences, probes derived from the human genes were used to detect the rat messages.
- ISIS 12633 (SEQ ID NO:78), a 20-mer phosphorothioate oligonucleotide complementary to a portion of the 3' UTR of rat c-jun mRNA, was selected as an active modulator of c-jun for further studies.
- Another preferred oligonucleotide targeted to rat AP-1 subunits is ISIS 12635 (SEQ ID NO:80).
- Tables 15 and 16 show the sequences and chemical modifications of second generation oligonucleotides designed to modulate mouse c-jun and c-fos mRNA expression. The activities of these modified oligonucleotide are evaluated as described infra in Example 8.
- RASM rat aortic smooth muscle
- PDGF ng/ml
- c-jun mRNA levels were markedly less in ISIS 12633-treated cells as compared to untreated cells or cells treated with ISIS 12898.
- the decrease in c-jun mRNA levels was associated with a significant decrease in the proportion of cells in the G2/M interface at 24 hours. This result provides evidence of the role of AP-1-mediated gene expression in cellular proliferation and indicate that cell cycle progression can be modulated by preventing expression of one or both of the genes which encode a subunit of AP-1.
- Invasion refers to the ability of cancer cells to detach from a primary site of attachment and penetrate, e.g., an underlying basement membrane.
- Metastasis indicates a sequence of events wherein (1) a cancer cell detaches from its extracellular matrices, (2) the detached cancer cell migrates to another portion of the patient's body, often via the circulatory system, and (3) attaches to a distal and inappropriate extracellular matrix, thereby created a focus from which a secondary tumor can arise.
- Normal cells do not possess the ability to invade or metastasize and/or undergo apoptosis (programmed cell death) if such events occur (Ruoslahti, Sci. Amer., 1996, 275, 72).
- MMPs matrix metalloproteinases
- the matrix metalloproteinases are a family of enzymes which have the ability to degrade components of the extracellular matrix (Birkedal-Hansen, Current Op. Biol., 1995, 7, 728). Many members of the MMP family have been found to have elevated levels of activity in human tumors as well as other disease states (Stetler-Stevenson et al., Annu. Rev. Cell Biol., 1993, 9, 541; Bernhard et al., Proc. Natl. Acad. Sci. (U.S.A.), 1994, 91, 4293).
- MMP-9 matrix metalloproteinase-9
- AP-1 transcription factor AP-1 transcription factor
- NHEKs normal human epidermal keratinocytes
- ISIS 10582 an oligonucleotide targeted to c-jun, was evaluated for its ability to modulate MMP-9 expression according to the protocols described in Examples 2-3 with the following exceptions: (1) NHEK cells were used instead of A549 cells, (2) the probe used, a PCR product prepared using the published sequence of the MMP-9 gene (Huhtala et al., J. Biol.
- Inducing agents other than TPA function to raise AP-1 levels in vivo.
- A549 cells were treated and evaluated as in Examples 2 et seq. with the exception that TNF-( ⁇ , IL-1 ⁇ or TNF- ⁇ or IL-1 ⁇ (each at 10 ng/ml and all from R&D Systems, Minneapolis, Minn.) were used in place of TPA as inducers.
- the results demonstrate that ISIS 10582 (SEQ ID NO:8, targeted to human c-jun) effectively reduces stimulation of c-Jun by TNF- ⁇ , IL-1 ⁇ or TGF- ⁇ .
- a scrambled control oligonucleotide, ISIS 11563 did not reverse the induction of c-Jun.
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Abstract
Description
TABLE 1
__________________________________________________________________________
Phosphorothioate Oligonucleotides Targeted to Human c-jun
TARGET
%
ISIS # SEQUENCE SEQ ID NO: REGION CONTROL*
__________________________________________________________________________
10570
GCC-ACA-CTC-AGT-GCA-ACT-CT
1 5' Cap
62
10571 CGC-ACC-TCC-ACT-CCC-GCC-TC 2 5'-UTR 100
10572 ACC-AGC-CCG-GGA-GCC-ACA-GG 3 5'-UTR 39
10578 GCT-GCG-CCG-CCG-ACG-TGA-CG 4 ORF 37
10579 CGC-CCC-GCC-GCC-GCT-GCT-CA 5 ORF 41
10580 GTG-TCT-CGC-CGG-GCA-TCT-CG 6 ORF 19
10581 CCC-CCG-ACG-GTC-TCT-CTT-CA 7 tTR 24
10582 TCA-GCC-CCC-GAC-GGT-CTC-TC 8 3'--UTR 17
10583 TGC-CCC-TCA-GCC-CCC-GAC-GG 9 3'--UTR 20
13305 TGC-GGG-TGA-GTG-GTA-G 118 ORF N.D. **
10582 Controls:
10582 TCA-GCC-CCC-GAC-GGT-CTC-TC 8 3'--UTR
11562 GAG-AGA-CCG-TCG-GGG-GCT-GA 29 sense control
11563 CAC-CTC-CAC-GCG-CTT-CTG-GC 30 scrambled control
11564 TCG-GCA-CCT-GAA-GGA-CTT-TC 31 mismatch control
__________________________________________________________________________
*Control is TPA induction, at 1 hour, in A549 cells.
** N.D., not determined.
TABLE 2
__________________________________________________________________________
Phosphorothioate Oligonucleotides Targeted to Human c-fos
TARGET
%
ISIS # SEQUENCE SEQ ID NO: REGION CONTROL*
__________________________________________________________________________
10628
TGC-TCG-CTG-CAG-ATG-CGG-TT
10 5' Cap
79
10629 CGG-TCA-CTG-CTC-GTT-CGC-TG 11 5'-UTR 72
10630 CAT-CGT-GGC-GGT-TAG-GCA-AA 12 tIR 91
10631 GAG-AAC-ATC-ATC-GTG-GCG-GT 13 tIR 118
10632 ACC-GTG-GGA-ATG-AAG-TTG-GC 14 ORF 63
10633 AGC-TCC-CTC-CTC-CGG-TTG-CG 15 ORF 24
10634 TTG-CAG-GCA-GGT-CGG-TGA-GC 16 ORF 42
10635 TGG-CAC-GGA-GCG-GGC-TGT-CT 17 ORF 12
10636 TGC-TGC-TGC-CCT-TGC-GGT-GG 18 ORF 42
10637 CCT-CAC-AGG-GCC-AGC-AGC-GT 19 tTR 35
10638 GGT-GCC-GGC-TGC-CTC-CCC-TT 20 3'-UTR 22
10639 AAG-TCC-TTG-AGG-CCC-ACA-GC 21 3'-UTR 9
10640 CCC-CTC-CAG-CAG-CTA-CCC-TT 22 3'-UTR 87
10641 TCC-CGT-CCC-CAG-AAG-CAG-TA 23 3'-UTR 68
10642 CGC-GCC-CGG-CCT-GAA-AAT-TT 24 3'-UTR 87
10643 CCT-GCC-TCG-GCC-TCC-CAA-AG 25 3'-UTR 39
10644 CCC-CCA-CTT-CCG-CCC-ACT-AT 26 3'-UTR 104
10645 TGG-TGC-CTG-CGT-GAT-ACT-CG 27 3'-UTR 56
10646 CCC-TCC-CAG-GCT-CAA-GTC-AT 28 3'-UTR 100
10639 Controls:
10639 AAG-TCC-TTG-AGG-CCC-ACA-GC 21 3'-UTR
11184 GCT-GTG-GGC-CTC-AAG-GAC-TT 32 sense control
11185 ATG-TGC-TAG-ATG-CGC-AAA-GT 33 mismatch control
11186 ACG-TCC-GAT-TCC-GAG-CGC-AA 34 scrambled control
11187 CAG-TGG-CCA-TCA-AAC-CCG-TG 35 scrambled control
__________________________________________________________________________
*Control is TPA induction, at 1 hour, in A549 cells.
TABLE 3
______________________________________
Dose-Response to Oligonucleotides Targeted to c-jun
OLIGONUCLEOTIDE
c-jun mRNA LEVELS
TREATMENT CONCENTRATION (% CONTROL)
______________________________________
None (basal level)
-- 31
Control* -- 100
TPA + ISIS 10582 50 nM 72
TPA + ISIS 10582 100 nM 45.5
TPA + ISIS 10582 200 nM 29.5
TPA + ISIS 10582 400 nM 16
______________________________________
*Control is TPA induction, at 1 hour, in A549 cells.
TABLE 4
______________________________________
Dose-Response to Oligonucleotides Targeted to c-fos
OLIGONUCLEOTIDE
c-fos mRNA LEVELS
TREATMENT CONCENTRATION (% CONTROL)
______________________________________
None (basal level)
-- 3
Control* -- 100
TPA + ISIS 10639 50 nM 64
TPA + ISIS 10639 100 nM 46
TPA + ISIS 10639 200 nM 20.5
TPA + ISIS 10639 400 nM 9
______________________________________
*Control is TPA induction, at 1 hour, in A549 cells.
TABLE 5
______________________________________
Specificity of c-fos and c-jun Oligonucleotides
Treatment c-fos c-jun
______________________________________
Basal 5 23
TPA-no oligo 100 100
10639: c-fos active 9 97
11184: c-fos sense 84 91
11185: c-fos mismatch 93 98
11186: c-fos scrambled 98 99
10582: c-jun active 91 4
11562: c-jun sense 89 87
11563: c-jun scrambled 99 93
11564: c-jun mismatch 99 71
______________________________________
TABLE 6
______________________________________
Response of Transplanted Tumors in Mice to
Oligonucleotides Targeted to c-jun
Mean Tumor
Treatment/Time Weight (g) Std. Dev. Std. Error
______________________________________
Saline:
Day 17 0.113 0.033 0.014
Day 20 0.177 0.045 0.019
Day 27 0.272 0.086 0.035
Day 34 0.560 0.293 0.120
ISIS 10639:
Day 17 0.105 0.035 0.014
Day 20 0.138 0.074 0.030
Day 27 0.225 0.070 0.028
Day 34 0.310 0.104 0.042
______________________________________
TABLE 7
______________________________________
Effect of c-fos Oligonucleotides on c-Fos Protein Levels
Treatment c-Fos
______________________________________
Basal 21
TPA-no oligo 100
10639: c-fos active 19
11184: c-fos sense 97
11185: c-fos mismatch 91
11186: c-fos scrambled 99
______________________________________
TABLE 8
__________________________________________________________________________
Additional Oligonucleotides and PNA Antisense Analogs Targeted to Human
AP-1 Subunits
SEQ
Oligonucleotide Sequence (5' -> 3') ID
ISIS # Target and Chemical Modifications* NO:
__________________________________________________________________________
C-JUN:
10570 & Derivatives:
10570 c-jun, 5' cap G.sup.S C.sup.S C.sup.S A.sup.S C.sup.S A.sup.S
C.sup.S T.sup.S C.sup.S
A.sup.S G.sup.S T.sup.S
G.sup.S C.sup.S A.sup.S
A.sup.S C.sup.S T.sup.S
C.sup.S T P═S 1
13306 c-jun, 5' cap
C.sup.S A.sup.S C.sup.S
T.sup.S C.sup.S A.sup.S
G.sup.S T.sup.S G.sup.S
C.sup.S A.sup.S A.sup.S
C.sup.S T.sup.S C.sup.S T
P═S 36
13297 c-jun, 5' cap C.sup.S A.sup.S C.sup.S T.sup.S C.sup.S A.sup.S
G.sup.S T.sup.S G.sup.S
C.sup.S A.sup.S A.sup.S
C.sup.S T.sup.S C.sup.S T
P═S/2'MO 36
12166 c-jun, 5' cap C.sup.N A.sup.N C.sup.N T.sup.N C.sup.N A.sup.N
G.sup.N T.sup.N G.sup.N
C.sup.N A.sup.N A.sup.N
C.sup.N T.sup.N C.sup.N
T.sup.N PNA(N) 36
13699 c-jun, 5' cap C.sup.N A.sup.N C.sup.N T.sup.K C.sup.N A.sup.N
G.sup.N T.sup.K G.sup.N
C.sup.N A.sup.N A.sup.N
C.sup.N T.sup.K C.sup.N
T.sup.K PNA(N) /Lys(K) 36
10579 & Derivatives:
10579 c-jun, ORF C.sup.S
G.sup.S C.sup.S C.sup.S
C.sup.S C.sup.S G.sup.S
C.sup.S C.sup.S G.sup.S
C.sup.S C.sup.S G.sup.S
C.sup.S T.sup.S G.sup.S
C.sup.S T.sup.S C.sup.S A
P═S 5
11567 c-jun, ORF C.sup.S G.sup.S C.sup.S C.sup.S C.sup.S C.sup.S
G.sup.S C.sup.S C.sup.S
G.sup.S C.sup.S C.sup.S
G.sup.S C.sup.S T.sup.S
G.sup.S C.sup.S T.sup.S
C.sup.S A 2'F 5
10571 & Derivatives:
10571 c-jun, 5'-UTR C.sup.S G.sup.S C.sup.S A.sup.S C.sup.S C.sup.S
T.sup.S C.sup.S C.sup.S
A.sup.S C.sup.S T.sup.S
C.sup.S C.sup.S C.sup.S
G.sup.S C.sup.S C.sup.S
T.sup.S C P═S 2
11568 c-jun, 5'-UTR
C.sup.S G.sup.S C.sup.S
A.sup.S C.sup.S C.sup.S
T.sup.S C.sup.S C.sup.S
A.sup.S C.sup.S T.sup.S
C.sup.S C.sup.S C.sup.S
G.sup.S C.sup.S C.sup.S
T.sup.S C 2'F 2
13307 c-jun, 5'-UTR C.sup.S C.sup.S T.sup.S C.sup.S C.sup.S A.sup.S
C.sup.S T.sup.S C.sup.S
C.sup.S C.sup.S G.sup.S
C.sup.S C.sup.S T.sup.S C
P═S 37
13296 c-jun, 5'-UTR C.sup.S C.sup.S T.sup.S C.sup.S C.sup.S A.sup.S
C.sup.S T.sup.S C.sup.S
C.sup.S C.sup.S G.sup.S
C.sup.S C.sup.S T.sup.S C
P═S/2'MO 37
12167 c-jun, 5'-UTR C.sup.N C.sup.N T.sup.N C.sup.N C.sup.N A.sup.N
C.sup.N T.sup.N C.sup.N
C.sup.N C.sup.N G.sup.N
C.sup.N C.sup.N T.sup.N
C.sup.N PNA(N) 37
13698 c-jun, 5'-UTR C.sup.N C.sup.N T.sup.K C.sup.N C.sup.N A.sup.N
C.sup.N T.sup.K C.sup.N
C.sup.N C.sup.N G.sup.N
C.sup.N C.sup.N T.sup.K
C.sup.N PNA(N) /Lys(K) 37
10582 & Derivatives:
10582 c-jun, 3'-UTR
T.sup.S C.sup.S A.sup.S
G.sup.S C.sup.S C.sup.S
C.sup.S C.sup.S C.sup.S
G.sup.S A.sup.S C.sup.S
G.sup.S G.sup.S T.sup.S
C.sup.S T.sup.S C.sup.S
T.sup.S C P═S 8
11569 c-jun, 3'-UTR
T.sup.S C.sup.S A.sup.S
G.sup.S C.sup.S C.sup.S
C.sup.S C.sup.S C.sup.S
G.sup.S A.sup.S C.sup.S
G.sup.S G.sup.S T.sup.S
C.sup.S T.sup.S C.sup.S
T.sup.S C 2'F 8
11537 c-jun, 3'-UTR T.sup.S C.sup.S A.sup.S G.sup.S C.sup.S C.sup.S
C.sup.S C.sup.S C.sup.S
G.sup.S A.sup.S C.sup.S
G.sup.S G.sup.S T.sup.S
C.sup.S T.sup.S C.sup.S
T.sup.S C 2'propoxy- 8
14314 c-jun, 3'-UTR
T.sup.S C.sup.S A.sup.S
G.sup.S C.sup.S C.sup.S
C.sup.S C.sup.S C.sup.S
G.sup.S A.sup.S C.sup.S
G.sup.S G.sup.S T.sup.S
C.sup.S T.sup.S C.sup.S
T.sup.S C 2'ME 8
C-FOS:
10639 & Derivatives:
10639 c-fos, 3'-UTR A.sup.S A.sup.S G.sup.S T.sup.S C.sup.S C.sup.S
T.sup.S T.sup.S G.sup.S
A.sup.S G.sup.S G.sup.S
C.sup.S C.sup.S C.sup.S
A.sup.S C.sup.S A.sup.S
G.sup.S C P═S 21
11200 c-fos, 3'-UTR
A.sup.S A.sup.S G.sup.S
T.sup.S C.sup.S C.sup.S
T.sup.S T.sup.S G.sup.S
A.sup.S G.sup.S G.sup.S
C.sup.S C.sup.S C.sup.S
A.sup.S C.sup.S A.sup.S
G.sup.S C 2'MO 21
11538 c-fos, 3'-UTR A.sup.S A.sup.S G.sup.S T.sup.S C.sup.S C.sup.S
T.sup.S T.sup.S G.sup.S
A.sup.S G.sup.S G.sup.S
C.sup.S C.sup.S C.sup.S
A.sup.S C.sup.S A.sup.S
G.sup.S C 2'propoxy- 21
14315 c-fos, 3'-UTR
A.sup.S A.sup.S G.sup.S
T.sup.S C.sup.S C.sup.S
T.sup.S T.sup.S G.sup.S
A.sup.S G.sup.S G.sup.S
C.sup.S C.sup.S C.sup.S
A.sup.S C.sup.S A.sup.S
G.sup.S C 2'ME 21
13298 & Derivatives:
13298 c-fos, ORF T.sup.S G.sup.S C.sup.S G.sup.S G.sup.S G.sup.S
T.sup.S G.sup.S A.sup.S
G.sup.S T.sup.S G.sup.S
G.sup.S T.sup.S A.sup.S G
2'ME 120
12165 c-fos, ORF T.sup.N G.sup.N C.sup.N G.sup.N G.sup.N G.sup.N
T.sup.N G.sup.N A.sup.N
G.sup.N T.sup.N G.sup.N
G.sup.N T.sup.N A.sup.N
G.sup.N PNA(N) 120
13646 c-fos, ORF T.sup.N
G.sup.N C.sup.N G.sup.N
G.sup.N G.sup.N T.sup.K
G.sup.N A.sup.N G.sup.N
T.sup.K G.sup.N G.sup.N
T.sup.K A.sup.N G.sup.N
PNA(N)/Lys(K) 120
10628 & Derivatives:
10628 c-fos, 5' cap T.sup.S G.sup.S C.sup.S T.sup.S C.sup.S G.sup.S
C.sup.S T.sup.S G.sup.S
C.sup.S A.sup.S G.sup.S
A.sup.S T.sup.S G.sup.S
C.sup.S G.sup.S G.sup.S
T.sup.S T P═S 10
13302 c-fos, 5' cap
C.sup.S G.sup.S C.sup.S
T.sup.S G.sup.S C.sup.S
A.sup.S G.sup.S A.sup.S
T.sup.S G.sup.S C.sup.S
G.sup.S G.sup.S T.sup.S T
P═S 121
13301 c-fos, 5' cap C.sup.S G.sup.S C.sup.S T.sup.S G.sup.S C.sup.S
A.sup.S G.sup.S A.sup.S
T.sup.S G.sup.S C.sup.S
G.sup.S G.sup.S T.sup.S T
P═S, 2'MO 121
12162 c-fos, 5' cap C.sup.N G.sup.N C.sup.N T.sup.N G.sup.N C.sup.N
A.sup.N G.sup.N A.sup.N
T.sup.N G.sup.N C.sup.N
G.sup.N G.sup.N T.sup.N T
PNA(N) 121
13643 c-fos, 5' cap C.sup.N G.sup.N C.sup.N T.sup.K G.sup.N C.sup.N
A.sup.N G.sup.N A.sup.N
T.sup.K G.sup.N C.sup.N
G.sup.N G.sup.N T.sup.K T
PNA(N) /Lys(K) 121
13303 & Derivatives:
13303 c-fos, 5'-UTR C.sup.S C.sup.S G.sup.S C.sup.S C.sup.S G.sup.S
G.sup.S C.sup.S T.sup.S
C.sup.S A.sup.S G.sup.S
T.sup.S C.sup.S T.sup.S T
P═S 122
13300 c-fos, 5'-UTR C.sup.S C.sup.S G.sup.S C.sup.S C.sup.S G.sup.S
G.sup.S C.sup.S T.sup.S
C.sup.S A.sup.S G.sup.S
T.sup.S C.sup.S T.sup.S T
P═S, 2'MO 122
12163 c-fos, 5'-UTR C.sup.N C.sup.N G.sup.N C.sup.N C.sup.N G.sup.N
G.sup.N C.sup.N T.sup.N
C.sup.N A.sup.N G.sup.N
T.sup.N C.sup.N T.sup.N
T.sup.N PNA(N) 122
13644 c-fos, 5'-UTR
C.sup.N C.sup.N G.sup.N
C.sup.N C.sup.N G.sup.N
G.sup.N C.sup.N T.sup.K
C.sup.N A.sup.N G.sup.N
T.sup.K C.sup.N T.sup.K
T.sup.K PNA(N)/Lys(K) 122
13304 & Derivatives:
13304 c-fos, tIR C.sup.S
A.sup.S T.sup.S C.sup.S
G.sup.S T.sup.S G.sup.S
G.sup.S C.sup.S G.sup.S
G.sup.S T.sup.S T.sup.S
A.sup.S G.sup.S G P═S
123
13299 c-fos, tIR C.sup.S A.sup.S T.sup.S C.sup.S G.sup.S T.sup.S
G.sup.S G.sup.S C.sup.S
G.sup.S G.sup.S T.sup.S
T.sup.S A.sup.S G.sup.S G
P═S, 2'MO 123
12164 c-fos, tIR C.sup.N A.sup.N T.sup.N C.sup.N G.sup.N T.sup.N
G.sup.N G.sup.N C.sup.N
G.sup.N G.sup.N T.sup.N
T.sup.N A.sup.N G.sup.N
G.sup.N PNA(N) 123
13700 c-fos, tIR C.sup.K
A.sup.N T.sup.K C.sup.K
G.sup.N T.sup.K G.sup.N
G.sup.N C.sup.K G.sup.N
G.sup.N T.sup.K T.sup.K
A.sup.N G.sup.N G.sup.K
PNA(N)/Lys(K) 123
14240 c-fos, tIR C.sup.K A.sup.N T.sup.K C.sup.K G.sup.N T.sup.K
G.sup.N G.sup.N C.sup.K
G.sup.N G.sup.N T.sup.K
T.sup.K A.sup.N G.sup.N
G.sup.K PNA(N) /Lys(K)/5'FIT
C 123
__________________________________________________________________________
*Phosphorothioate linkages are indicated by ".sup.S " and "P═S";
emboldened residues indicate the additional indicated modifications:
2'F = 2fluoro-;
2'propoxy =2propoxy-;
2'MO = 2methoxy-;
2'ME = 2methoxyethoxy-;
PNA = peptide (polyamide) nucleic acid backbone having a side chain
corresponding to that of either glycine (N) or DLys (K);
5'FITC = 5fluorescein isothiocyanate.
TABLE 9
__________________________________________________________________________
5-Methyl-Cytosine, Fully 2'-Methoxyethoxy-Oligonucleotides
Targeted to the 3'-UTR of Human c-fos
ISIS SEQ ID
NO. SEQUENCE NO.
__________________________________________________________________________
15828
C.sup.O C.sup.O A.sup.O T.sup.O C.sup.O T.sup.O T.sup.O A.sup.O
A.sup.O T.sup.O A.sup.O A.sup.O A.sup.O T.sup.O A.sup.O A.sup.O
A.sup.O T.sup.O T.sup.O A.sup.O A.sup.O A.sup.O A.sup.O A.sup.O
C.sup.O A.sup.O C.sup.O A.sup.O A.sup.O T
131
14660 A.sup.O A.sup.O A.sup.O T.sup.O A.sup.O A.sup.O A.sup.O T.sup.O
T.sup.O A.sup.O A.sup.O
A.sup.O A.sup.O A.sup.O
C.sup.O A.sup.O C.sup.O
A.sup.O A.sup.O T 2,6-A* 132
14659 A.sup.O A.sup.O T.sup.O
T.sup.O A.sup.O A.sup.O
A.sup.O A.sup.O A.sup.O
C.sup.O A.sup.O C.sup.O
A.sup.O A.sup.O T.sup.O
A.sup.O A.sup.O A.sup.O
A.sup.O C 2,6-A 133
15829 A.sup.O T.sup.O A.sup.O T.sup.O A.sup.O A.sup.O A.sup.O T.sup.O
A.sup.O T.sup.O C.sup.O
T.sup.O G.sup.O A.sup.O
G.sup.O A.sup.O A.sup.O
T.sup.O C.sup.O C 134
14662 A.sup.O T.sup.O A.sup.O T.sup.O A.sup.O A.sup.O A.sup.O T.sup.O
A.sup.O T.sup.O C.sup.O
T.sup.O G.sup.O A.sup.O
G.sup.O A.sup.O A.sup.O
T.sup.O C.sup.O C 2,6-A 135
14661 A.sup.O T.sup.O C.sup.O
T.sup.O G.sup.O A.sup.O
G.sup.O A.sup.O A.sup.O
T.sup.O C.sup.O C.sup.O
A.sup.O T.sup.O C.sup.O
T.sup.O T.sup.O A.sup.O
A.sup.O T 2,6-A 136
14663** A.sup.O A.sup.O A.sup.O T.sup.O A.sup.O T.sup.O A.sup.O A.sup.O
A.sup.O T.sup.O A.sup.O
T.sup.O C.sup.O T.sup.O
G.sup.O A.sup.O G.sup.O
A.sup.O A.sup.O T 2,6-A 137
14664 A.sup.O A.sup.O G.sup.O
A.sup.O C.sup.O C.sup.O
T.sup.O C.sup.O A.sup.O
A.sup.O G.sup.O G.sup.O
T.sup.O A.sup.O G.sup.O
A.sup.O A.sup.O A.sup.O
A.sup.O A 138
__________________________________________________________________________
*Emboldened residues indicate 2,6A residues, i.e., those having
2,6diaminopurine as a nucleobase.
**ISIS 14663 is a 2deoxy- rather than a 2methoxyethoxy-oligonucleotide.
TABLE 10
______________________________________
Effect of Modified c-fos Oligonucleotides on c-fos Expression
Treatment c-fos
______________________________________
Basal 3
TPA-no oligo 100
10639: c-fos active, P═S 9
11200: c-fos, 2'-fluoro- 5
11538: c-fos, 2'-propoxy- 15
______________________________________
TABLE 11
__________________________________________________________________________
Phosphorothioate Oligonucleotides Targeted to Mouse c-jun
ISIS #
SEQUENCE SEQ ID NO:
TARGET REGION*
__________________________________________________________________________
12292
CTC-GCC-CAA-CTT-CAG-CCG-CC
38 5'-UTR: 434-453
12293 CCA-GTC-CCA-GCA-ACA-GCG-GC 39 5'-UTR: 588-607
12294 GCA-ACA-GCG-CGC-CGG-GAA-GC 40 5'-UTR: 838-857
12295 CCG-GCG-ACG-CCA-GCT-TGA-GC 41 ORF: 1120-1139
12296 GGC-TGT-GCC-GCG-GAG-GTG-AC 42 ORF: 1304-1323
12297 CGC-CCC-ACC-GCC-GCT-GCT-CA 43 ORF: 1458-1477
12298 AGC-CCG-GCC-GCG-CCA-TAG-GA 44 ORF: 1481-1500
12299 CTG-CAC-CGG-GAT-CTG-TTG-GG 45 ORF: 1560-1579
12300 GGC-GGC-GTC-TCT-CCC-GGC-ATC-TC 46 ORF: 1625-1647
12301 TGG-AGG-CGG-CAA-TGC-GGT-TC 47 ORF: 1708-1727
12302 CCC-TGA-GCA-TGT-TGG-CCG-TG 48 ORF: 1813-1832
12303 CAA-AGC-CAG-GCG-CGC-CAC-GT 49 3'-UTR: 2096-2115
12304 TTG-AGA-GAG-GCA-GGC-CAG-GG 50 3'-UTR: 2388-2407
12305 TGG-ACT-TGT-GTG-TTG-CCG-GG 51 3'-UTR: 2807-2826
12306 TCC-ATG-GGT-CCC-TGC-TTT-GA 52 3'-UTR: 2999-3018
12321 TGG-TCG-CGC-GCG-GGC-ACA-GC 53 3'-UTR: 2166-2185
__________________________________________________________________________
*Nucleotide coordinates from Genbank accession No. J04115/MUSCJUN.
TABLE 12
__________________________________________________________________________
Phosphorothioate Oligonucleotides Targeted to Mouse c-fos
ISIS #
SEQUENCE SEQ ID NO:
TARGET REGION*
__________________________________________________________________________
11249
AGC-TCC-CTC-CTC-CGA-TTC-CG
54 ORF: 1905-1924
11250 GCT-CTG-TGA-CCA-TGG-GCC-CC 55 ORF: 2498-2517
12307 GAA-CCG-CCG-GCT-CTA-TCC-AG 56 5'-UTR: 164-183
12308 GCC-CCT-GCG-AGT-CAC-ACC-CC 57 ORF: 485-504
12309 TAA-GGC-TGC-TCT-GAC-CGC-GC 58 ORF: 541-560
12310 CGC-CCG-CAG-CAC-CCT-CCT-CC 59 ORF: 804-823
12311 CAG-GCG-CTG-CTC-CGG-AGT-CT 60 ORF: 868-887
12312 TCC-CTT-GAA-TTC-CGC-AGC-GC 61 ORF: 989-1008
12313 AGC-GGA-GGT-GAG-CGA-GGA-GG 62 ORF: 1136-1155
12314 CCC-CAG-CCC-ACA-AAG-GTC-CA 63 ORF: 1445-1464
12315 TGC-TCA-AGG-ACC-CTG-CGC-CC 64 ORF: 2001-2020
12316 GGG-AAG-CCA-AGG-TCA-TCG-GG 65 ORF: 2178-2197
12317 TGC-TGC-TGC-CCT-TTC-GGT-GG 66 ORF: 2630-2649
12318 CTG-GAT-GCC-GGC-TGC-CTT-GC 67 3'-UTR: 2716-2735
12319 CAG-CTC-GGG-CAG-TGG-CAC-GT 68 3'-UTR: 2736-2755
12320 GGA-ACA-CGC-TAT-TGC-CAG-GA 69 3'-UTR: 3138-3157
__________________________________________________________________________
*Nucleotide coordinates from Genbank accession No. J00370/MUSFOS.
TABLE 13
__________________________________________________________________________
Phosphorothioate Oligonucleotides Targeted to Rat c-jun
ISIS #
SEQUENCE SEQ ID NO:
TARGET REGION*
__________________________________________________________________________
12624
CGG-CGG-CGC-AGA-CCA-GTC-GT
70 5'-UTR: 2-21
12625 GCC-GCG-GGA-CCA-GCC-CCA-GC 119 5'-UTR: 35-54
12626 GGC-ATC-GTC-GTA-GAA-GGT-CG 71 5'-UTR: 20-39
12627 GGA-GGT-GCG-GCT-TCA-GAT-TG 72 ORF: 493-512
12628 CCC-TCC-TGC-TCG-TCG-GTC-AC 73 5'-UTR: 307-326
12629 ACT-GAC-TGG-TTG-TGC-CGC-GG 74 ORF: 747-766
12630 CGC-TGT-AGC-CGC-CGC-CGC-CG 75 ORF: 814-833
12631 CCT-TGA-TCC-GCT-CCT-GAG-AC 76 ORF: 1105-1124
12632 GCC-AGC-TCG-GAG-TTT-TGC-GC 77 ORF: 1226-1245
12633 TTT-TCT-TCC-ACT-GCC-CCT-CA 78 3'-UTR: 1375-1394
12634 CCC-TTG-GCT-TCA-GTA-CTC-GG 79 3'-UTR: 1451-1470
12635 CTT-CCC-ACT-CCA-GCA-CAT-TG 80 3'-UTR: 1509-1528
12636 GCA-CAG-CCC-GTT-CGC-AAA-GC 81 3'-UTR: 1584-1603
12637 AAT-GCA-GCA-GAG-AGG-TTG-GG 82 3'-UTR: 2089-2108
12638 GAC-GGG-AGG-GAC-TAC-AGG-CT 83 3'-UTR: 2168-2187
12639 TCT-GGA-CTT-GTG-GGT-TGC-TG 84 3'-UTR: 2240-2259
12640 TAA-ACG-ATC-ACA-GCG-CAT-GC 85 3'-UTR: 2375-2394
12628 control:
12628 CCC-TCC-TGC-TCG-TCG-GTC-AC 73 5'-UTR
12893 GGG-AGG-ACG-AGC-AGC-CAG-TG 86 reverse sense control
12894 CCC-GGC-CTT-TTG-ACC-GCC-TC 87 scrambled control
12895 CCG-CCT-CCC-CGG-CCT-TTT-GA 88 scrambled control
12896 CCG-TCG-TGG-TCC-TCC-GTG-AC 89 mismatch control
12992 GTG-ACC-GAC-GAG-CAG-GAG-GG 90 sense control
12633 control:
12633 TTT-TCT-TCC-ACT-GCC-CCT-CA 78 3'-UTR
12897 AAA-AGA-AGG-TGA-CGG-GGA-GT 91 reverse sense control
12898 TTC-TCT-TTT-AGC-CTC-CCC-CA 92 scrambled control
12899 TCC-CCC-ATT-CTC-TTT-TAG-CC 93 scrambled control
12900 TTA-TCA-TCG-ACA-GCG-CCA-CA 94 mismatch control
12993 TGA-GGG-GCA-GTG-GAA-GAA-AA 95 sense control
__________________________________________________________________________
*Nucleotide coordinates from Genbank accession No. X17163/RSJUNAP1.
TABLE 14
__________________________________________________________________________
Phosphorothioate Oligonucleotides Targeted to Rat c-fos
ISIS #
SEQUENCE SEQ ID NO:
TARGET REGION*
__________________________________________________________________________
11124
GTT-CTC-GGC-TCC-GCC-GGC-TC
96 5'-UTR: 22-41
11245 CAT-CAT-GGT-CGT-GGT-TTG-GG 97 tIR: 122-140
12246 TCC-GCG-TTG-AAA-CCC-GAG-AA 98 ORF: 141-160
12247 TGG-GCT-GGT-GGA-GAT-GGC-TG 99 ORF: 328-347
12248 CGA-TGC-TCT-GCG-CTC-TGC-CG 100 ORF: 485-504
12251 TTC-GGT-GGG-CAG-CTG-CGC-AG 101 ORF: 1193-1212
12252 CAG-GGC-TAG-CAG-TGT-GGG-CG 102 tTR: 1255-1274
12253 CCA-GCT-CAG-TCA-GTG-CCG-GC 103 3'-UTR: 1299-1318
12254 TCT-ACG-GGA-ACC-CCT-CGA-GG 104 3'-UTR: 1348-1367
12255 CTC-CAT-GCG-GTT-GCT-TTT-GA 105 3'-UTR: 1518-1537
12256 CAG-GCC-TGG-CTC-ACA-TGC-TA 106 3'-UTR: 1576-1595
11254 controls:
11254 TCT-ACG-GGA-ACC-CCT-CGA-GG 104 3'-UTR
12698 AGA-TGC-CCT-TGG-GGA-GCT-CC 107 reverse sense control
12699 TGA-CTA-TAG-ACC-GCC-GCC-GG 108 scrambled control
12700 CCG-CCG-GTG-ACT-ATA-GAC-CG 109 scrambled control
12728 TCA-ACC-GGT-ACG-CCA-CGT-GG 110 mismatch control
12990 CCT-CGA-GGG-GTT-CCC-GTA-GA 111 sense control
11256 controls:
11256 CAG-GCC-TGG-CTC-ACA-TGC-TA 106
12701 GTC-CGG-ACC-GAG-TGT-ACG-AT 112 reverse sense control
12702 GCG-CAC-CGT-CAT-TAC-GTC-GA 113 scrambled control
12703 ACG-TCG-AGC-GCA-CCG-TCA-TT 114 scrambled control
12729 CAC-GCG-TGC-CTG-ACT-TGG-TA 115 mismatch control
12991 TAG-CAT-GTG-AGC-CAG-GCC-TG 116 sense control
__________________________________________________________________________
*Nucleotide coordinates from Genbank accession No. X06769/RNCFOSR (see
also Curran et al., Oncogene, 1987, 2:79).
TABLE 15
__________________________________________________________________________
Additional Oligonucleotides Targeted to Rat c-jun
Oligonucleotide Sequence (5' -> 3')
SEQ ID
ISIS # Target and Chemical Modifications* NO:
__________________________________________________________________________
12633 &
Derivatives:
12633 3'-UTR T.sup.S T.sup.S T.sup.S T.sup.S C.sup.S T.sup.S T.sup.S
C.sup.S C.sup.S A.sup.S
C.sup.S T.sup.S G.sup.S
C.sup.S C.sup.S C.sup.S
C.sup.S T.sup.S C.sup.S A 78
13047 3'-UTR T.sup.O T.sup.O
T.sup.O T.sup.O C.sup.O
T.sup.S T.sup.S C.sup.S
C.sup.S A.sup.S C.sup.S
T.sup.S G.sup.S C.sup.S
C.sup.O C.sup.O C.sup.O
T.sup.O C.sup.O A.sup.d 2'MO
78
13714 3'-UTR T.sup.O T.sup.O T.sup.O T.sup.O C.sup.O T.sup.S T.sup.S
C.sup.S C.sup.S A.sup.S
C.sup.S T.sup.S G.sup.S
C.sup.S C.sup.O C.sup.O
C.sup.O T.sup.O C.sup.O
A.sup.d 2'ME 78
15707 3'-UTR T.sup.S T.sup.S T.sup.S T.sup.S C.sup.O T.sup.O T.sup.O
C.sup.O C.sup.O A.sup.O
C.sup.O T.sup.O G.sup.O
C.sup.O C.sup.O C.sup.S
C.sup.S T.sup.S C.sup.S
A.sup.d 2'ME 78
15708 3'-UTR T.sup.S T.sup.S T.sup.S T.sup.S C.sup.S T.sup.O T.sup.O
C.sup.O C.sup.O A.sup.O
C.sup.O T.sup.O G.sup.O
C.sup.O C.sup.S C.sup.S
C.sup.S T.sup.S C.sup.S
A.sup.d 2'ME 78
13881 3'-UTR T.sup.O T.sup.O T.sup.O T.sup.O C.sup.O T.sup.O T.sup.O
C.sup.O C.sup.O A.sup.O
C.sup.O T.sup.O G.sup.S
C.sup.S C.sup.S C.sup.S
C.sup.S T.sup.S C.sup.S
A.sup.d 2'ME 78
13882 3'-UTR T.sup.S T.sup.S T.sup.S T.sup.S C.sup.S T.sup.S T.sup.S
C.sup.S C.sup.O A.sup.O
C.sup.O T.sup.O G.sup.O
C.sup.O C.sup.O C.sup.O
C.sup.O T.sup.O C.sup.O
A.sup.d 2'ME 78
12898 (scrambled 12633) & Derivatives:
12898 control T.sup.S T.sup.S C.sup.S T.sup.S C.sup.S T.sup.S T.sup.S
T.sup.S T.sup.S A.sup.S
G.sup.S C.sup.S C.sup.S
T.sup.S C.sup.S C.sup.S
C.sup.S C.sup.S C.sup.S A 92
13046 control T.sup.O
T.sup.O C.sup.O T.sup.O
C.sup.O T.sup.S T.sup.S
T.sup.S T.sup.S A.sup.S
G.sup.S C.sup.S C.sup.S
T.sup.S C.sup.O C.sup.O
C.sup.O C.sup.O C.sup.O
A.sup.d 2'MO 92
13715 control T.sup.O T.sup.O C.sup.O T.sup.O C.sup.O T.sup.S T.sup.S
T.sup.S T.sup.S A.sup.S
G.sup.S C.sup.S C.sup.S
T.sup.S C.sup.O C.sup.O
C.sup.O C.sup.O C.sup.O
A.sup.d 2'ME 92
13912 control T.sup.O T.sup.O C.sup.O T.sup.O C.sup.O T.sup.O T.sup.O
T.sup.O T.sup.O A.sup.O
G.sup.O C.sup.O C.sup.S
T.sup.S C.sup.S C.sup.S
C.sup.S C.sup.S C.sup.S
A.sup.d 2'ME 92
13913 control T.sup.S T.sup.S C.sup.S T.sup.S C.sup.S T.sup.S T.sup.S
T.sup.S T.sup.O A.sup.O
G.sup.O C.sup.O C.sup.O
T.sup.O C.sup.O C.sup.O
C.sup.O C.sup.O C.sup.O
A.sup.d 2'ME 92
15705 control T.sup.S T.sup.S C.sup.S T.sup.S C.sup.O T.sup.O T.sup.O
T.sup.O T.sup.O A.sup.O
G.sup.O C.sup.O C.sup.O
T.sup.O C.sup.O C.sup.S
C.sup.S C.sup.S C.sup.S
A.sup.d 2'ME 92
15706 control T.sup.S T.sup.S C.sup.S T.sup.S C.sup.O T.sup.O T.sup.O
T.sup.O T.sup.O A.sup.O
G.sup.O C.sup.O C.sup.O
T.sup.O C.sup.O C.sup.O
C.sup.S C.sup.S C.sup.S
A.sup.d 2'ME 92
12628 & Derivatives:
12628 5'-UTR C.sup.S C.sup.S C.sup.S T.sup.S C.sup.S C.sup.S T.sup.S
G.sup.S C.sup.S T.sup.S
C.sup.S G.sup.S T.sup.S
C.sup.S G.sup.S G.sup.S
T.sup.S C.sup.S A.sup.S C 73
13049 5'-UTR C.sup.O C.sup.O
C.sup.O T.sup.O C.sup.O
C.sup.S T.sup.S G.sup.S
C.sup.S T.sup.S C.sup.S
G.sup.S T.sup.S C.sup.S
G.sup.O G.sup.O T.sup.O
C.sup.O A.sup.O C.sup.d 2'MO
73
13712 5'-UTR C.sup.O C.sup.O C.sup.O T.sup.O C.sup.O C.sup.S T.sup.S
G.sup.S C.sup.S T.sup.S
C.sup.S G.sup.S T.sup.S
C.sup.S G.sup.O G.sup.O
T.sup.O C.sup.O A.sup.O
C.sup.d 2'ME 73
13879 5'-UTR C.sup.O C.sup.O C.sup.O T.sup.O C.sup.O C.sup.O T.sup.O
G.sup.O C.sup.O T.sup.O
C.sup.O G.sup.S T.sup.S
C.sup.S G.sup.S G.sup.S
T.sup.S C.sup.S A.sup.S
C.sup.d 2'ME 73
13880 5'-UTR C.sup.S C.sup.S C.sup.S T.sup.S C.sup.S C.sup.S T.sup.S
G.sup.S C.sup.O T.sup.O
C.sup.O G.sup.O T.sup.O
C.sup.O G.sup.O G.sup.O
T.sup.O C.sup.O A.sup.O
C.sup.d 2'ME 73
12894 (scrambled 12628) & Derivatives:
12894 C.sup.S C.sup.S C.sup.S G.sup.S G.sup.S C.sup.S C.sup.S T.sup.S
T.sup.S T.sup.S T.sup.S
G.sup.S A.sup.S C.sup.S
C.sup.S G.sup.S C.sup.S
C.sup.S T.sup.S C 87
13713 C.sup.O C.sup.O C.sup.O G.sup.O G.sup.O C.sup.S C.sup.S T.sup.S
T.sup.S T.sup.S T.sup.S
G.sup.S A.sup.S C.sup.S
C.sup.O G.sup.O C.sup.O
C.sup.O T.sup.O C.sup.d 2'ME
87
13048 C.sup.O C.sup.O C.sup.O G.sup.O G.sup.O C.sup.S C.sup.S T.sup.S
T.sup.S T.sup.S T.sup.S
G.sup.S A.sup.S C.sup.S
C.sup.O G.sup.C C.sup.O
C.sup.O T.sup.O C.sup.d 2'MO
87
12635 & Derivatives:
12635 C.sup.S T.sup.S T.sup.S C.sup.S C.sup.S C.sup.S A.sup.S C.sup.S
T.sup.S C.sup.S C.sup.S
A.sup.S G.sup.S C.sup.S
A.sup.S C.sup.S A.sup.S
T.sup.S T.sup.S G 80
15711 C.sup.S T.sup.S T.sup.S C.sup.S C.sup.S C.sup.S A.sup.S C.sup.S
T.sup.S C.sup.S C.sup.S
A.sup.S G.sup.S C.sup.S
A.sup.S C.sup.S A.sup.S
T.sup.S T.sup.S G 2'ME 80
15712 C.sup.S T.sup.S
T.sup.S C.sup.S C.sup.S
C.sup.S A.sup.S C.sup.S
T.sup.S C.sup.S C.sup.S
A.sup.S G.sup.S C.sup.S
A.sup.S C.sup.S A.sup.S
T.sup.S T.sup.S G.sup.d 2'ME
80
15709 (scrambled 12635) & Derivatives:
15709 T.sup.S T.sup.S C.sup.S T.sup.S C.sup.S A.sup.S C.sup.S C.sup.S
C.sup.S A.sup.S C.sup.S
C.sup.S A.sup.S C.sup.S
G.sup.S T.sup.S A.sup.S
C.sup.S G.sup.S T 2'ME 117
15710 T.sup.S T.sup.S
C.sup.S T.sup.S C.sup.O
A.sup.O C.sup.O C.sup.O
C.sup.O A.sup.O C.sup.O
C.sup.O A.sup.O C.sup.O
G.sup.O T.sup.S A.sup.S
C.sup.S G.sup.S T 2'ME
__________________________________________________________________________
117
*Phosphorothioate linkages are indicated by ".sup.S ", whereas
phosphodiester linkages are signified by ".sup.O ", emboldened residues
comprise the additional indicated modifications:
2'MO = 2methoxy-;
2ME = 2methoxyethoxy-.
TABLE 16
__________________________________________________________________________
Additional Oligonucleotides Targeted to Rat c-fos
Oligonucleotide Sequence (5' -> 3').
SEQ ID
ISIS # Target and Chemical Modifications* NO:
__________________________________________________________________________
11256
& Derivatives: 106
11256 3'-UTR C.sup.S A.sup.S G.sup.S G.sup.S C.sup.S C.sup.S T.sup.S
G.sup.S G.sup.S C.sup.S
T.sup.S C.sup.S A.sup.S
C.sup.S A.sup.S T.sup.S
G.sup.S C.sup.S T.sup.S A 106
13051 3'-UTR C.sup.O A.sup.O G.sup.O G.sup.O C.sup.O C.sup.S T.sup.S
G.sup.S G.sup.S C.sup.S
T.sup.S C.sup.S A.sup.S
C.sup.S A.sup.O T.sup.O
G.sup.O C.sup.O T.sup.O
A.sup.d 2'MO 106
13718 3'-UTR C.sup.S A.sup.S G.sup.S G.sup.S C.sup.S C.sup.S T.sup.S
G.sup.S G.sup.S C.sup.S
T.sup.S C.sup.S A.sup.S
C.sup.S A.sup.S T.sup.S
G.sup.S C.sup.S T.sup.S
A.sup.d 2'ME 106
13877 3'-UTR C.sup.O A.sup.O G.sup.O G.sup.O C.sup.O C.sup.O T.sup.O
G.sup.O G.sup.O C.sup.O
T.sup.O C.sup.O A.sup.S
C.sup.S A.sup.S T.sup.S
G.sup.S C.sup.S T.sup.S
A.sup.d 2'ME 106
13878 3'-UTR C.sup.O A.sup.O G.sup.O G.sup.O C.sup.O C.sup.O T.sup.O
G.sup.O G.sup.S C.sup.S
T.sup.S C.sup.S A.sup.S
C.sup.S A.sup.S T.sup.S
G.sup.S C.sup.S T.sup.S
A.sup.d 2'ME 106
12703 (Scrambled 11256) & Derivatives:
12703 control A.sup.S C.sup.S G.sup.S T.sup.S C.sup.S G.sup.S A.sup.S
G.sup.S C.sup.S G.sup.S
C.sup.S A.sup.S C.sup.S
C.sup.S G.sup.S T.sup.S
C.sup.S A.sup.S T.sup.S T 114
13050 control A.sup.O C.sup.O G.sup.C T.sup.O C.sup.O G.sup.S A.sup.S
G.sup.S C.sup.S G.sup.S
C.sup.S A.sup.S C.sup.S
C.sup.S G.sup.O T.sup.O
C.sup.O A.sup.O T.sup.O
T.sup.d 2'MO 114
13719 control A.sup.S C.sup.S G.sup.S T.sup.S C.sup.S G.sup.S A.sup.S
G.sup.S C.sup.S G.sup.S
C.sup.S A.sup.S C.sup.S
C.sup.S G.sup.S T.sup.S
C.sup.S A.sup.S T.sup.S
T.sup.d 2'ME 114
11254 & Derivatives:
11254 3'-UTR T.sup.S C.sup.S T.sup.S A.sup.S C.sup.S G.sup.S G.sup.S
G.sup.S A.sup.S A.sup.S
C.sup.S C.sup.S C.sup.S
C.sup.S T.sup.S C.sup.S
G.sup.S A.sup.S G.sup.S G 104
13053 3'-UTR T.sup.O C.sup.O T.sup.O A.sup.O C.sup.O G.sup.S G.sup.S
G.sup.S A.sup.S A.sup.S
C.sup.S C.sup.S C.sup.S
C.sup.S T.sup.O C.sup.O
G.sup.O A.sup.O G.sup.O
G.sup.d 2'MO 104
13716 3'-UTR T.sup.S C.sup.S T.sup.S A.sup.S C.sup.S G.sup.S G.sup.S
G.sup.S A.sup.S A.sup.S
C.sup.S C.sup.S C.sup.S
C.sup.S T.sup.S C.sup.S
G.sup.S A.sup.S G.sup.S
G.sup.d 2'ME 104
13875 3'-UTR T.sup.O C.sup.O T.sup.O A.sup.O C.sup.O G.sup.O G.sup.O
G.sup.O A.sup.O A.sup.O
C.sup.O C.sup.O C.sup.S
C.sup.S T.sup.S C.sup.S
G.sup.S A.sup.S G.sup.S
G.sup.d 2'ME 104
13876 3'-UTR T.sup.S C.sup.S T.sup.S A.sup.S C.sup.S G.sup.S G.sup.S
G.sup.S A.sup.O A.sup.O
C.sup.O C.sup.O C.sup.O
C.sup.O T.sup.O C.sup.O
G.sup.O A.sup.O G.sup.O
G.sup.d 2'ME 104
12700 (Scrambled 11254) & Derivatives:
12700 control C.sup.S C.sup.S G.sup.S C.sup.S C.sup.S G.sup.S G.sup.S
T.sup.S G.sup.S A.sup.S
C.sup.S T.sup.S A.sup.S
T.sup.S A.sup.S G.sup.S
A.sup.S C.sup.S C.sup.S G 109
13052 control C.sup.O C.sup.O G.sup.O C.sup.O C.sup.O G.sup.S G.sup.S
T.sup.S G.sup.S A.sup.S
C.sup.S T.sup.S A.sup.S
T.sup.S A.sup.O G.sup.O
A.sup.O C.sup.O C.sup.O
G.sup.d 2'MO 109
13717 control C.sup.S C.sup.S G.sup.S C.sup.S C.sup.S G.sup.S G.sup.S
T.sup.S G.sup.S A.sup.S
C.sup.S T.sup.S A.sup.S
T.sup.S A.sup.S G.sup.S
A.sup.S C.sup.S C.sup.S
G.sup.d 2'ME 109
__________________________________________________________________________
*Phosphorothioate and phosphodiester linkages are indicated by ".sup.S "
and ".sup.O ", respectively, whereas ".sup.d " indicates a dideoxy
(chainterminating) residue; emboldened residues comprise the additional
indicated modifications:
2'MO, 2methoxy; 2'ME, 2methoxyethoxy-.
TABLE 17
______________________________________
Effect of c-jun Oligonucleotide on MMP-9 Expression
Treatment MMP-9
______________________________________
Basal 4
TPA - no oligo 100
10582: c-jun active 6
11562: sense control 99
11563: scrambled control 95
11564: mismatch control 89
______________________________________
TABLE 18
______________________________________
Effect of Oligonucleotides Targeted to c-Jun
on Induction by TNF-α, IL-1β or TGF-β
ISIS ISIS
Inducer Basal No Oligo 10582 11563
______________________________________
TNF-α
5 100 20 98
IL-1β 9 100 15 94
TGF-β 2 100 95 99
______________________________________
__________________________________________________________________________
# SEQUENCE LISTING
- - - - (1) GENERAL INFORMATION:
- - (iii) NUMBER OF SEQUENCES: 139
- - - - (2) INFORMATION FOR SEQ ID NO:1:
- - (i) SEQUENCE CHARACTERISTICS:
(A) LENGTH: 20
(B) TYPE: Nucleic Acid
(C) STRANDEDNESS: Single
(D) TOPOLOGY: Linear
- - (iv) ANTI-SENSE: Yes
- - (xi) SEQUENCE DESCRIPTION: SEQ ID NO: - # 1:
- - GCCACACTCA GTGCAACTCT - # - #
- # 20
- - - - (2) INFORMATION FOR SEQ ID NO: 2:
- - (i) SEQUENCE CHARACTERISTICS:
(A) LENGTH: 20
(B) TYPE: Nucleic Acid
(C) STRANDEDNESS: Single
(D) TOPOLOGY: Linear
- - (iv) ANTI-SENSE: Yes
- - (xi) SEQUENCE DESCRIPTION: SEQ ID NO: - # 2:
- - CGCACCTCCA CTCCCGCCTC - # - #
- # 20
- - - - (2) INFORMATION FOR SEQ ID NO: 3:
- - (i) SEQUENCE CHARACTERISTICS:
(A) LENGTH: 20
(B) TYPE: Nucleic Acid
(C) STRANDEDNESS: Single
(D) TOPOLOGY: Linear
- - (iv) ANTI-SENSE: Yes
- - (xi) SEQUENCE DESCRIPTION: SEQ ID NO: - # 3:
- - ACCAGCCCGG GAGCCACAGG - # - #
- # 20
- - - - (2) INFORMATION FOR SEQ ID NO: 4:
- - (i) SEQUENCE CHARACTERISTICS:
(A) LENGTH: 20
(B) TYPE: Nucleic Acid
(C) STRANDEDNESS: Single
(D) TOPOLOGY: Linear
- - (iv) ANTI-SENSE: Yes
- - (xi) SEQUENCE DESCRIPTION: SEQ ID NO: - # 4:
- - GCTGCGCCGC CGACGTGACG - # - #
- # 20
- - - - (2) INFORMATION FOR SEQ ID NO: 5:
- - (i) SEQUENCE CHARACTERISTICS:
(A) LENGTH: 20
(B) TYPE: Nucleic Acid
(C) STRANDEDNESS: Single
(D) TOPOLOGY: Linear
- - (iv) ANTI-SENSE: Yes
- - (xi) SEQUENCE DESCRIPTION: SEQ ID NO: - # 5:
- - CGCCCCGCCG CCGCTGCTCA - # - #
- # 20
- - - - (2) INFORMATION FOR SEQ ID NO: 6:
- - (i) SEQUENCE CHARACTERISTICS:
(A) LENGTH: 20
(B) TYPE: Nucleic Acid
(C) STRANDEDNESS: Single
(D) TOPOLOGY: Linear
- - (iv) ANTI-SENSE: Yes
- - (xi) SEQUENCE DESCRIPTION: SEQ ID NO: - # 6:
- - GTGTCTCGCC GGGCATCTCG - # - #
- # 20
- - - - (2) INFORMATION FOR SEQ ID NO: 7:
- - (i) SEQUENCE CHARACTERISTICS:
(A) LENGTH: 20
(B) TYPE: Nucleic Acid
(C) STRANDEDNESS: Single
(D) TOPOLOGY: Linear
- - (iv) ANTI-SENSE: Yes
- - (xi) SEQUENCE DESCRIPTION: SEQ ID NO: - # 7:
- - CCCCCGACGG TCTCTCTTCA - # - #
- # 20
- - - - (2) INFORMATION FOR SEQ ID NO: 8:
- - (i) SEQUENCE CHARACTERISTICS:
(A) LENGTH: 20
(B) TYPE: Nucleic Acid
(C) STRANDEDNESS: Single
(D) TOPOLOGY: Linear
- - (iv) ANTI-SENSE: Yes
- - (xi) SEQUENCE DESCRIPTION: SEQ ID NO: - # 8:
- - TCAGCCCCCG ACGGTCTCTC - # - #
- # 20
- - - - (2) INFORMATION FOR SEQ ID NO: 9:
- - (i) SEQUENCE CHARACTERISTICS:
(A) LENGTH: 20
(B) TYPE: Nucleic Acid
(C) STRANDEDNESS: Single
(D) TOPOLOGY: Linear
- - (iv) ANTI-SENSE: Yes
- - (xi) SEQUENCE DESCRIPTION: SEQ ID NO: - # 9:
- - TGCCCCTCAG CCCCCGACGG - # - #
- # 20
- - - - (2) INFORMATION FOR SEQ ID NO: 10:
- - (i) SEQUENCE CHARACTERISTICS:
(A) LENGTH: 20
(B) TYPE: Nucleic Acid
(C) STRANDEDNESS: Single
(D) TOPOLOGY: Linear
- - (iv) ANTI-SENSE: Yes
- - (xi) SEQUENCE DESCRIPTION: SEQ ID NO: - # 10:
- - TGCTCGCTGC AGATGCGGTT - # - #
- # 20
- - - - (2) INFORMATION FOR SEQ ID NO: 11:
- - (i) SEQUENCE CHARACTERISTICS:
(A) LENGTH: 20
(B) TYPE: Nucleic Acid
(C) STRANDEDNESS: Single
(D) TOPOLOGY: Linear
- - (iv) ANTI-SENSE: Yes
- - (xi) SEQUENCE DESCRIPTION: SEQ ID NO: - # 11:
- - CGGTCACTGC TCGTTCGCTG - # - #
- # 20
- - - - (2) INFORMATION FOR SEQ ID NO: 12:
- - (i) SEQUENCE CHARACTERISTICS:
(A) LENGTH: 20
(B) TYPE: Nucleic Acid
(C) STRANDEDNESS: Single
(D) TOPOLOGY: Linear
- - (iv) ANTI-SENSE: Yes
- - (xi) SEQUENCE DESCRIPTION: SEQ ID NO: - # 12:
- - CATCGTGGCG GTTAGGCAAA - # - #
- # 20
- - - - (2) INFORMATION FOR SEQ ID NO: 13:
- - (i) SEQUENCE CHARACTERISTICS:
(A) LENGTH: 20
(B) TYPE: Nucleic Acid
(C) STRANDEDNESS: Single
(D) TOPOLOGY: Linear
- - (iv) ANTI-SENSE: Yes
- - (xi) SEQUENCE DESCRIPTION: SEQ ID NO: - # 13:
- - GAGAACATCA TCGTGGCGGT - # - #
- # 20
- - - - (2) INFORMATION FOR SEQ ID NO: 14:
- - (i) SEQUENCE CHARACTERISTICS:
(A) LENGTH: 20
(B) TYPE: Nucleic Acid
(C) STRANDEDNESS: Single
(D) TOPOLOGY: Linear
- - (iv) ANTI-SENSE: Yes
- - (xi) SEQUENCE DESCRIPTION: SEQ ID NO: - # 14:
- - ACCGTGGGAA TGAAGTTGGC - # - #
- # 20
- - - - (2) INFORMATION FOR SEQ ID NO: 15:
- - (i) SEQUENCE CHARACTERISTICS:
(A) LENGTH: 20
(B) TYPE: Nucleic Acid
(C) STRANDEDNESS: Single
(D) TOPOLOGY: Linear
- - (iv) ANTI-SENSE: Yes
- - (xi) SEQUENCE DESCRIPTION: SEQ ID NO: - # 15:
- - AGCTCCCTCC TCCGGTTGCG - # - #
- # 20
- - - - (2) INFORMATION FOR SEQ ID NO: 16:
- - (i) SEQUENCE CHARACTERISTICS:
(A) LENGTH: 20
(B) TYPE: Nucleic Acid
(C) STRANDEDNESS: Single
(D) TOPOLOGY: Linear
- - (iv) ANTI-SENSE: Yes
- - (xi) SEQUENCE DESCRIPTION: SEQ ID NO: - # 16:
- - TTGCAGGCAG GTCGGTGAGC - # - #
- # 20
- - - - (2) INFORMATION FOR SEQ ID NO: 17:
- - (i) SEQUENCE CHARACTERISTICS:
(A) LENGTH: 20
(B) TYPE: Nucleic Acid
(C) STRANDEDNESS: Single
(D) TOPOLOGY: Linear
- - (iv) ANTI-SENSE: Yes
- - (xi) SEQUENCE DESCRIPTION: SEQ ID NO: - # 17:
- - TGGCACGGAG CGGGCTGTCT - # - #
- # 20
- - - - (2) INFORMATION FOR SEQ ID NO: 18:
- - (i) SEQUENCE CHARACTERISTICS:
(A) LENGTH: 20
(B) TYPE: Nucleic Acid
(C) STRANDEDNESS: Single
(D) TOPOLOGY: Linear
- - (iv) ANTI-SENSE: Yes
- - (xi) SEQUENCE DESCRIPTION: SEQ ID NO: - # 18:
- - TGCTGCTGCC CTTGCGGTGG - # - #
- # 20
- - - - (2) INFORMATION FOR SEQ ID NO: 19:
- - (i) SEQUENCE CHARACTERISTICS:
(A) LENGTH: 20
(B) TYPE: Nucleic Acid
(C) STRANDEDNESS: Single
(D) TOPOLOGY: Linear
- - (iv) ANTI-SENSE: Yes
- - (xi) SEQUENCE DESCRIPTION: SEQ ID NO: - # 19:
- - CCTCACAGGG CCAGCAGCGT - # - #
- # 20
- - - - (2) INFORMATION FOR SEQ ID NO: 20:
- - (i) SEQUENCE CHARACTERISTICS:
(A) LENGTH: 20
(B) TYPE: Nucleic Acid
(C) STRANDEDNESS: Single
(D) TOPOLOGY: Linear
- - (iv) ANTI-SENSE: Yes
- - (xi) SEQUENCE DESCRIPTION: SEQ ID NO: - # 20:
- - GGTGCCGGCT GCCTCCCCTT - # - #
- # 20
- - - - (2) INFORMATION FOR SEQ ID NO: 21:
- - (i) SEQUENCE CHARACTERISTICS:
(A) LENGTH: 20
(B) TYPE: Nucleic Acid
(C) STRANDEDNESS: Single
(D) TOPOLOGY: Linear
- - (iv) ANTI-SENSE: Yes
- - (xi) SEQUENCE DESCRIPTION: SEQ ID NO: - # 21:
- - AAGTCCTTGA GGCCCACAGC - # - #
- # 20
- - - - (2) INFORMATION FOR SEQ ID NO: 22:
- - (i) SEQUENCE CHARACTERISTICS:
(A) LENGTH: 20
(B) TYPE: Nucleic Acid
(C) STRANDEDNESS: Single
(D) TOPOLOGY: Linear
- - (iv) ANTI-SENSE: Yes
- - (xi) SEQUENCE DESCRIPTION: SEQ ID NO: - # 22:
- - CCCCTCCAGC AGCTACCCTT - # - #
- # 20
- - - - (2) INFORMATION FOR SEQ ID NO: 23:
- - (i) SEQUENCE CHARACTERISTICS:
(A) LENGTH: 20
(B) TYPE: Nucleic Acid
(C) STRANDEDNESS: Single
(D) TOPOLOGY: Linear
- - (iv) ANTI-SENSE: Yes
- - (xi) SEQUENCE DESCRIPTION: SEQ ID NO: - # 23:
- - TCCCGTCCCC AGAAGCAGTA - # - #
- # 20
- - - - (2) INFORMATION FOR SEQ ID NO: 24:
- - (i) SEQUENCE CHARACTERISTICS:
(A) LENGTH: 20
(B) TYPE: Nucleic Acid
(C) STRANDEDNESS: Single
(D) TOPOLOGY: Linear
- - (iv) ANTI-SENSE: Yes
- - (xi) SEQUENCE DESCRIPTION: SEQ ID NO: - # 24:
- - CGCGCCCGGC CTGAAAATTT - # - #
- # 20
- - - - (2) INFORMATION FOR SEQ ID NO: 25:
- - (i) SEQUENCE CHARACTERISTICS:
(A) LENGTH: 20
(B) TYPE: Nucleic Acid
(C) STRANDEDNESS: Single
(D) TOPOLOGY: Linear
- - (iv) ANTI-SENSE: Yes
- - (xi) SEQUENCE DESCRIPTION: SEQ ID NO: - # 25:
- - CCTGCCTCGG CCTCCCAAAG - # - #
- # 20
- - - - (2) INFORMATION FOR SEQ ID NO: 26:
- - (i) SEQUENCE CHARACTERISTICS:
(A) LENGTH: 20
(B) TYPE: Nucleic Acid
(C) STRANDEDNESS: Single
(D) TOPOLOGY: Linear
- - (iv) ANTI-SENSE: Yes
- - (xi) SEQUENCE DESCRIPTION: SEQ ID NO: - # 26:
- - CCCCCACTTC CGCCCACTAT - # - #
- # 20
- - - - (2) INFORMATION FOR SEQ ID NO: 27:
- - (i) SEQUENCE CHARACTERISTICS:
(A) LENGTH: 20
(B) TYPE: Nucleic Acid
(C) STRANDEDNESS: Single
(D) TOPOLOGY: Linear
- - (iv) ANTI-SENSE: Yes
- - (xi) SEQUENCE DESCRIPTION: SEQ ID NO: - # 27:
- - TGGTGCCTGC GTGATACTCG - # - #
- # 20
- - - - (2) INFORMATION FOR SEQ ID NO: 28:
- - (i) SEQUENCE CHARACTERISTICS:
(A) LENGTH: 20
(B) TYPE: Nucleic Acid
(C) STRANDEDNESS: Single
(D) TOPOLOGY: Linear
- - (iv) ANTI-SENSE: Yes
- - (xi) SEQUENCE DESCRIPTION: SEQ ID NO: - # 28:
- - CCCTCCCAGG CTCAAGTCAT - # - #
- # 20
- - - - (2) INFORMATION FOR SEQ ID NO: 29:
- - (i) SEQUENCE CHARACTERISTICS:
(A) LENGTH: 20
(B) TYPE: Nucleic Acid
(C) STRANDEDNESS: Single
(D) TOPOLOGY: Linear
- - (iv) ANTI-SENSE: No
- - (xi) SEQUENCE DESCRIPTION: SEQ ID NO: - # 29:
- - GAGAGACCGT CGGGGGCTGA - # - #
- # 20
- - - - (2) INFORMATION FOR SEQ ID NO:30:
- - (i) SEQUENCE CHARACTERISTICS:
(A) LENGTH: 20
(B) TYPE: Nucleic Acid
(C) STRANDEDNESS: Single
(D) TOPOLOGY: Linear
- - (iv) ANTI-SENSE: No
- - (xi) SEQUENCE DESCRIPTION: SEQ ID NO: - # 30:
- - CACCTCCACG CGCTTCTGGC - # - #
- # 20
- - - - (2) INFORMATION FOR SEQ ID NO: 31:
- - (i) SEQUENCE CHARACTERISTICS:
(A) LENGTH: 20
(B) TYPE: Nucleic Acid
(C) STRANDEDNESS: Single
(D) TOPOLOGY: Linear
- - (iv) ANTI-SENSE: Yes
- - (xi) SEQUENCE DESCRIPTION: SEQ ID NO: - # 31:
- - TCGGCACCTG AAGGACTTTC - # - #
- # 20
- - - - (2) INFORMATION FOR SEQ ID NO: 32:
- - (i) SEQUENCE CHARACTERISTICS:
(A) LENGTH: 20
(B) TYPE: Nucleic Acid
(C) STRANDEDNESS: Single
(D) TOPOLOGY: Linear
- - (iv) ANTI-SENSE: No
- - (xi) SEQUENCE DESCRIPTION: SEQ ID NO: - # 32:
- - GCTGTGGGCC TCAAGGACTT - # - #
- # 20
- - - - (2) INFORMATION FOR SEQ ID NO: 33:
- - (i) SEQUENCE CHARACTERISTICS:
(A) LENGTH: 20
(B) TYPE: Nucleic Acid
(C) STRANDEDNESS: Single
(D) TOPOLOGY: Linear
- - (iv) ANTI-SENSE: Yes
- - (xi) SEQUENCE DESCRIPTION: SEQ ID NO: - # 33:
- - ATGTGCTAGA TGCGCAAAGT - # - #
- # 20
- - - - (2) INFORMATION FOR SEQ ID NO: 34:
- - (i) SEQUENCE CHARACTERISTICS:
(A) LENGTH: 20
(B) TYPE: Nucleic Acid
(C) STRANDEDNESS: Single
(D) TOPOLOGY: Linear
- - (iv) ANTI-SENSE: No
- - (xi) SEQUENCE DESCRIPTION: SEQ ID NO: - # 34:
- - ACGTCCGATT CCGAGCGCAA - # - #
- # 20
- - - - (2) INFORMATION FOR SEQ ID NO: 35:
- - (i) SEQUENCE CHARACTERISTICS:
(A) LENGTH: 20
(B) TYPE: Nucleic Acid
(C) STRANDEDNESS: Single
(D) TOPOLOGY: Linear
- - (iv) ANTI-SENSE: Yes
- - (xi) SEQUENCE DESCRIPTION: SEQ ID NO: - # 35:
- - CAGTGGCCAT CAAACCCGTG - # - #
- # 20
- - - - (2) INFORMATION FOR SEQ ID NO: 36:
- - (i) SEQUENCE CHARACTERISTICS:
(A) LENGTH: 16
(B) TYPE: Nucleic Acid
(C) STRANDEDNESS: Single
(D) TOPOLOGY: Linear
- - (iv) ANTI-SENSE: Yes
- - (xi) SEQUENCE DESCRIPTION: SEQ ID NO: - # 36:
- - CACTCAGTGC AACTCT - # - #
- # 16
- - - - (2) INFORMATION FOR SEQ ID NO: 37:
- - (i) SEQUENCE CHARACTERISTICS:
(A) LENGTH: 16
(B) TYPE: Nucleic Acid
(C) STRANDEDNESS: Single
(D) TOPOLOGY: Linear
- - (iv) ANTI-SENSE: Yes
- - (xi) SEQUENCE DESCRIPTION: SEQ ID NO: - # 37:
- - CCTCCACTCC CGCCTC - # - #
- # 16
- - - - (2) INFORMATION FOR SEQ ID NO: 38:
- - (i) SEQUENCE CHARACTERISTICS:
(A) LENGTH: 20
(B) TYPE: Nucleic Acid
(C) STRANDEDNESS: Single
(D) TOPOLOGY: Linear
- - (iv) ANTI-SENSE: Yes
- - (xi) SEQUENCE DESCRIPTION: SEQ ID NO: - # 38:
- - CTCGCCCAAC TTCAGCCGCC - # - #
- # 20
- - - - (2) INFORMATION FOR SEQ ID NO: 39:
- - (i) SEQUENCE CHARACTERISTICS:
(A) LENGTH: 20
(B) TYPE: Nucleic Acid
(C) STRANDEDNESS: Single
(D) TOPOLOGY: Linear
- - (iv) ANTI-SENSE: Yes
- - (xi) SEQUENCE DESCRIPTION: SEQ ID NO: - # 39:
- - CCAGTCCCAG CAACAGCGGC - # - #
- # 20
- - - - (2) INFORMATION FOR SEQ ID NO: 40:
- - (i) SEQUENCE CHARACTERISTICS:
(A) LENGTH: 20
(B) TYPE: Nucleic Acid
(C) STRANDEDNESS: Single
(D) TOPOLOGY: Linear
- - (iv) ANTI-SENSE: Yes
- - (xi) SEQUENCE DESCRIPTION: SEQ ID NO: - # 40:
- - GCAACAGCGC GCCGGGAAGC - # - #
- # 20
- - - - (2) INFORMATION FOR SEQ ID NO: 41:
- - (i) SEQUENCE CHARACTERISTICS:
(A) LENGTH: 20
(B) TYPE: Nucleic Acid
(C) STRANDEDNESS: Single
(D) TOPOLOGY: Linear
- - (iv) ANTI-SENSE: Yes
- - (xi) SEQUENCE DESCRIPTION: SEQ ID NO: - # 41:
- - CCGGCGACGC CAGCTTGAGC - # - #
- # 20
- - - - (2) INFORMATION FOR SEQ ID NO: 42:
- - (i) SEQUENCE CHARACTERISTICS:
(A) LENGTH: 20
(B) TYPE: Nucleic Acid
(C) STRANDEDNESS: Single
(D) TOPOLOGY: Linear
- - (iv) ANTI-SENSE: Yes
- - (xi) SEQUENCE DESCRIPTION: SEQ ID NO: - # 42:
- - GGCTGTGCCG CGGAGGTGAC - # - #
- # 20
- - - - (2) INFORMATION FOR SEQ ID NO: 43:
- - (i) SEQUENCE CHARACTERISTICS:
(A) LENGTH: 20
(B) TYPE: Nucleic Acid
(C) STRANDEDNESS: Single
(D) TOPOLOGY: Linear
- - (iv) ANTI-SENSE: Yes
- - (xi) SEQUENCE DESCRIPTION: SEQ ID NO: - # 43:
- - CGCCCCACCG CCGCTGCTCA - # - #
- # 20
- - - - (2) INFORMATION FOR SEQ ID NO: 44:
- - (i) SEQUENCE CHARACTERISTICS:
(A) LENGTH: 20
(B) TYPE: Nucleic Acid
(C) STRANDEDNESS: Single
(D) TOPOLOGY: Linear
- - (iv) ANTI-SENSE: Yes
- - (xi) SEQUENCE DESCRIPTION: SEQ ID NO: - # 44:
- - AGCCCGGCCG CGCCATAGGA - # - #
- # 20
- - - - (2) INFORMATION FOR SEQ ID NO: 45:
- - (i) SEQUENCE CHARACTERISTICS:
(A) LENGTH: 20
(B) TYPE: Nucleic Acid
(C) STRANDEDNESS: Single
(D) TOPOLOGY: Linear
- - (iv) ANTI-SENSE: Yes
- - (xi) SEQUENCE DESCRIPTION: SEQ ID NO: - # 45:
- - CTGCACCGGG ATCTGTTGGG - # - #
- # 20
- - - - (2) INFORMATION FOR SEQ ID NO: 46:
- - (i) SEQUENCE CHARACTERISTICS:
(A) LENGTH: 23
(B) TYPE: Nucleic Acid
(C) STRANDEDNESS: Single
(D) TOPOLOGY: Linear
- - (iv) ANTI-SENSE: Yes
- - (xi) SEQUENCE DESCRIPTION: SEQ ID NO: - # 46:
- - GGCGGCGTCT CTCCCGGCAT CTC - # - #
23
- - - - (2) INFORMATION FOR SEQ ID NO: 47:
- - (i) SEQUENCE CHARACTERISTICS:
(A) LENGTH: 20
(B) TYPE: Nucleic Acid
(C) STRANDEDNESS: Single
(D) TOPOLOGY: Linear
- - (iv) ANTI-SENSE: Yes
- - (xi) SEQUENCE DESCRIPTION: SEQ ID NO: - # 47:
- - TGGAGGCGGC AATGCGGTTC - # - #
- # 20
- - - - (2) INFORMATION FOR SEQ ID NO: 48:
- - (i) SEQUENCE CHARACTERISTICS:
(A) LENGTH: 20
(B) TYPE: Nucleic Acid
(C) STRANDEDNESS: Single
(D) TOPOLOGY: Linear
- - (iv) ANTI-SENSE: Yes
- - (xi) SEQUENCE DESCRIPTION: SEQ ID NO: - # 48:
- - CCCTGAGCAT GTTGGCCGTG - # - #
- # 20
- - - - (2) INFORMATION FOR SEQ ID NO: 49:
- - (i) SEQUENCE CHARACTERISTICS:
(A) LENGTH: 20
(B) TYPE: Nucleic Acid
(C) STRANDEDNESS: Single
(D) TOPOLOGY: Linear
- - (iv) ANTI-SENSE: Yes
- - (xi) SEQUENCE DESCRIPTION: SEQ ID NO: - # 49:
- - CAAAGCCAGG CGCGCCACGT - # - #
- # 20
- - - - (2) INFORMATION FOR SEQ ID NO: 50:
- - (i) SEQUENCE CHARACTERISTICS:
(A) LENGTH: 20
(B) TYPE: Nucleic Acid
(C) STRANDEDNESS: Single
(D) TOPOLOGY: Linear
- - (iv) ANTI-SENSE: Yes
- - (xi) SEQUENCE DESCRIPTION: SEQ ID NO: - # 50:
- - TTGAGAGAGG CAGGCCAGGG - # - #
- # 20
- - - - (2) INFORMATION FOR SEQ ID NO: 51:
- - (i) SEQUENCE CHARACTERISTICS:
(A) LENGTH: 20
(B) TYPE: Nucleic Acid
(C) STRANDEDNESS: Single
(D) TOPOLOGY: Linear
- - (iv) ANTI-SENSE: Yes
- - (xi) SEQUENCE DESCRIPTION: SEQ ID NO: - # 51:
- - TGGACTTGTG TGTTGCCGGG - # - #
- # 20
- - - - (2) INFORMATION FOR SEQ ID NO: 52:
- - (i) SEQUENCE CHARACTERISTICS:
(A) LENGTH: 20
(B) TYPE: Nucleic Acid
(C) STRANDEDNESS: Single
(D) TOPOLOGY: Linear
- - (iv) ANTI-SENSE: Yes
- - (xi) SEQUENCE DESCRIPTION: SEQ ID NO: - # 52:
- - TCCATGGGTC CCTGCTTTGA - # - #
- # 20
- - - - (2) INFORMATION FOR SEQ ID NO: 53:
- - (i) SEQUENCE CHARACTERISTICS:
(A) LENGTH: 20
(B) TYPE: Nucleic Acid
(C) STRANDEDNESS: Single
(D) TOPOLOGY: Linear
- - (iv) ANTI-SENSE: Yes
- - (xi) SEQUENCE DESCRIPTION: SEQ ID NO: - # 53:
- - TGGTCGCGCG CGGGCACAGC - # - #
- # 20
- - - - (2) INFORMATION FOR SEQ ID NO: 54:
- - (i) SEQUENCE CHARACTERISTICS:
(A) LENGTH: 20
(B) TYPE: Nucleic Acid
(C) STRANDEDNESS: Single
(D) TOPOLOGY: Linear
- - (iv) ANTI-SENSE: Yes
- - (xi) SEQUENCE DESCRIPTION: SEQ ID NO: - # 54:
- - AGCTCCCTCC TCCGATTCCG - # - #
- # 20
- - - - (2) INFORMATION FOR SEQ ID NO: 55:
- - (i) SEQUENCE CHARACTERISTICS:
(A) LENGTH: 20
(B) TYPE: Nucleic Acid
(C) STRANDEDNESS: Single
(D) TOPOLOGY: Linear
- - (iv) ANTI-SENSE: Yes
- - (xi) SEQUENCE DESCRIPTION: SEQ ID NO: - # 55:
- - GCTCTGTGAC CATGGGCCCC - # - #
- # 20
- - - - (2) INFORMATION FOR SEQ ID NO: 56:
- - (i) SEQUENCE CHARACTERISTICS:
(A) LENGTH: 20
(B) TYPE: Nucleic Acid
(C) STRANDEDNESS: Single
(D) TOPOLOGY: Linear
- - (iv) ANTI-SENSE: Yes
- - (xi) SEQUENCE DESCRIPTION: SEQ ID NO: - # 56:
- - GAACCGCCGG CTCTATCCAG - # - #
- # 20
- - - - (2) INFORMATION FOR SEQ ID NO: 57:
- - (i) SEQUENCE CHARACTERISTICS:
(A) LENGTH: 20
(B) TYPE: Nucleic Acid
(C) STRANDEDNESS: Single
(D) TOPOLOGY: Linear
- - (iv) ANTI-SENSE: Yes
- - (xi) SEQUENCE DESCRIPTION: SEQ ID NO: - # 57:
- - GCCCCTGCGA GTCACACCCC - # - #
- # 20
- - - - (2) INFORMATION FOR SEQ ID NO: 58:
- - (i) SEQUENCE CHARACTERISTICS:
(A) LENGTH: 20
(B) TYPE: Nucleic Acid
(C) STRANDEDNESS: Single
(D) TOPOLOGY: Linear
- - (iv) ANTI-SENSE: Yes
- - (xi) SEQUENCE DESCRIPTION: SEQ ID NO: - # 58:
- - TAAGGCTGCT CTGACCGCGC - # - #
- # 20
- - - - (2) INFORMATION FOR SEQ ID NO: 59:
- - (i) SEQUENCE CHARACTERISTICS:
(A) LENGTH: 20
(B) TYPE: Nucleic Acid
(C) STRANDEDNESS: Single
(D) TOPOLOGY: Linear
- - (iv) ANTI-SENSE: Yes
- - (xi) SEQUENCE DESCRIPTION: SEQ ID NO: - # 59:
- - CGCCCGCAGC ACCCTCCTCC - # - #
- # 20
- - - - (2) INFORMATION FOR SEQ ID NO: 60:
- - (i) SEQUENCE CHARACTERISTICS:
(A) LENGTH: 20
(B) TYPE: Nucleic Acid
(C) STRANDEDNESS: Single
(D) TOPOLOGY: Linear
- - (iv) ANTI-SENSE: Yes
- - (xi) SEQUENCE DESCRIPTION: SEQ ID NO: - # 60:
- - CAGGCGCTGC TCCGGAGTCT - # - #
- # 20
- - - - (2) INFORMATION FOR SEQ ID NO: 61:
- - (i) SEQUENCE CHARACTERISTICS:
(A) LENGTH: 20
(B) TYPE: Nucleic Acid
(C) STRANDEDNESS: Single
(D) TOPOLOGY: Linear
- - (iv) ANTI-SENSE: Yes
- - (xi) SEQUENCE DESCRIPTION: SEQ ID NO: - # 61:
- - TCCCTTGAAT TCCGCAGCGC - # - #
- # 20
- - - - (2) INFORMATION FOR SEQ ID NO: 62:
- - (i) SEQUENCE CHARACTERISTICS:
(A) LENGTH: 20
(B) TYPE: Nucleic Acid
(C) STRANDEDNESS: Single
(D) TOPOLOGY: Linear
- - (iv) ANTI-SENSE: Yes
- - (xi) SEQUENCE DESCRIPTION: SEQ ID NO: - # 62:
- - AGCGGAGGTG AGCGAGGAGG - # - #
- # 20
- - - - (2) INFORMATION FOR SEQ ID NO: 63:
- - (i) SEQUENCE CHARACTERISTICS:
(A) LENGTH: 20
(B) TYPE: Nucleic Acid
(C) STRANDEDNESS: Single
(D) TOPOLOGY: Linear
- - (iv) ANTI-SENSE: Yes
- - (xi) SEQUENCE DESCRIPTION: SEQ ID NO: - # 63:
- - CCCCAGCCCA CAAAGGTCCA - # - #
- # 20
- - - - (2) INFORMATION FOR SEQ ID NO: 64:
- - (i) SEQUENCE CHARACTERISTICS:
(A) LENGTH: 20
(B) TYPE: Nucleic Acid
(C) STRANDEDNESS: Single
(D) TOPOLOGY: Linear
- - (iv) ANTI-SENSE: Yes
- - (xi) SEQUENCE DESCRIPTION: SEQ ID NO: - # 64:
- - TGCTCAAGGA CCCTGCGCCC - # - #
- # 20
- - - - (2) INFORMATION FOR SEQ ID NO: 65:
- - (i) SEQUENCE CHARACTERISTICS:
(A) LENGTH: 20
(B) TYPE: Nucleic Acid
(C) STRANDEDNESS: Single
(D) TOPOLOGY: Linear
- - (iv) ANTI-SENSE: Yes
- - (xi) SEQUENCE DESCRIPTION: SEQ ID NO: - # 65:
- - GGGAAGCCAA GGTCATCGGG - # - #
- # 20
- - - - (2) INFORMATION FOR SEQ ID NO: 66:
- - (i) SEQUENCE CHARACTERISTICS:
(A) LENGTH: 20
(B) TYPE: Nucleic Acid
(C) STRANDEDNESS: Single
(D) TOPOLOGY: Linear
- - (iv) ANTI-SENSE: Yes
- - (xi) SEQUENCE DESCRIPTION: SEQ ID NO: - # 66:
- - TGCTGCTGCC CTTTCGGTGG - # - #
- # 20
- - - - (2) INFORMATION FOR SEQ ID NO: 67:
- - (i) SEQUENCE CHARACTERISTICS:
(A) LENGTH: 20
(B) TYPE: Nucleic Acid
(C) STRANDEDNESS: Single
(D) TOPOLOGY: Linear
- - (iv) ANTI-SENSE: Yes
- - (xi) SEQUENCE DESCRIPTION: SEQ ID NO: - # 67:
- - CTGGATGCCG GCTGCCTTGC - # - #
- # 20
- - - - (2) INFORMATION FOR SEQ ID NO: 68:
- - (i) SEQUENCE CHARACTERISTICS:
(A) LENGTH: 20
(B) TYPE: Nucleic Acid
(C) STRANDEDNESS: Single
(D) TOPOLOGY: Linear
- - (iv) ANTI-SENSE: Yes
- - (xi) SEQUENCE DESCRIPTION: SEQ ID NO: - # 68:
- - CAGCTCGGGA AGTGGCACGT - # - #
- # 20
- - - - (2) INFORMATION FOR SEQ ID NO: 69:
- - (i) SEQUENCE CHARACTERISTICS:
(A) LENGTH: 20
(B) TYPE: Nucleic Acid
(C) STRANDEDNESS: Single
(D) TOPOLOGY: Linear
- - (iv) ANTI-SENSE: Yes
- - (xi) SEQUENCE DESCRIPTION: SEQ ID NO: - # 69:
- - GGAACACGCT ATTGCCAGGA - # - #
- # 20
- - - - (2) INFORMATION FOR SEQ ID NO: 70:
- - (i) SEQUENCE CHARACTERISTICS:
(A) LENGTH: 20
(B) TYPE: Nucleic Acid
(C) STRANDEDNESS: Single
(D) TOPOLOGY: Linear
- - (iv) ANTI-SENSE: Yes
- - (xi) SEQUENCE DESCRIPTION: SEQ ID NO: - # 70:
- - CGGCGGCGCA GACCAGTCGT - # - #
- # 20
- - - - (2) INFORMATION FOR SEQ ID NO: 71:
- - (i) SEQUENCE CHARACTERISTICS:
(A) LENGTH: 20
(B) TYPE: Nucleic Acid
(C) STRANDEDNESS: Single
(D) TOPOLOGY: Linear
- - (iv) ANTI-SENSE: Yes
- - (xi) SEQUENCE DESCRIPTION: SEQ ID NO: - # 71:
- - GGCATCGTCG TAGAAGGTCG - # - #
- # 20
- - - - (2) INFORMATION FOR SEQ ID NO: 72:
- - (i) SEQUENCE CHARACTERISTICS:
(A) LENGTH: 20
(B) TYPE: Nucleic Acid
(C) STRANDEDNESS: Single
(D) TOPOLOGY: Linear
- - (iv) ANTI-SENSE: Yes
- - (xi) SEQUENCE DESCRIPTION: SEQ ID NO: - # 72:
- - GGAGGTGCGG CTTCAGATTG - # - #
- # 20
- - - - (2) INFORMATION FOR SEQ ID NO: 73:
- - (i) SEQUENCE CHARACTERISTICS:
(A) LENGTH: 20
(B) TYPE: Nucleic Acid
(C) STRANDEDNESS: Single
(D) TOPOLOGY: Linear
- - (iv) ANTI-SENSE: Yes
- - (xi) SEQUENCE DESCRIPTION: SEQ ID NO: - # 73:
- - CCCTCCTGCT CGTCGGTCAC - # - #
- # 20
- - - - (2) INFORMATION FOR SEQ ID NO: 74:
- - (i) SEQUENCE CHARACTERISTICS:
(A) LENGTH: 20
(B) TYPE: Nucleic Acid
(C) STRANDEDNESS: Single
(D) TOPOLOGY: Linear
- - (iv) ANTI-SENSE: Yes
- - (xi) SEQUENCE DESCRIPTION: SEQ ID NO: - # 74:
- - ACTGACTGGT TGTGCCGCGG - # - #
- # 20
- - - - (2) INFORMATION FOR SEQ ID NO: 75:
- - (i) SEQUENCE CHARACTERISTICS:
(A) LENGTH: 20
(B) TYPE: Nucleic Acid
(C) STRANDEDNESS: Single
(D) TOPOLOGY: Linear
- - (iv) ANTI-SENSE: Yes
- - (xi) SEQUENCE DESCRIPTION: SEQ ID NO: - # 75:
- - CGCTGTAGCC GCCGCCGCCG - # - #
- # 20
- - - - (2) INFORMATION FOR SEQ ID NO: 76:
- - (i) SEQUENCE CHARACTERISTICS:
(A) LENGTH: 20
(B) TYPE: Nucleic Acid
(C) STRANDEDNESS: Single
(D) TOPOLOGY: Linear
- - (iv) ANTI-SENSE: Yes
- - (xi) SEQUENCE DESCRIPTION: SEQ ID NO: - # 76:
- - CCTTGATCCG CTCCTGAGAC - # - #
- # 20
- - - - (2) INFORMATION FOR SEQ ID NO: 77:
- - (i) SEQUENCE CHARACTERISTICS:
(A) LENGTH: 20
(B) TYPE: Nucleic Acid
(C) STRANDEDNESS: Single
(D) TOPOLOGY: Linear
- - (iv) ANTI-SENSE: Yes
- - (xi) SEQUENCE DESCRIPTION: SEQ ID NO: - # 77:
- - GCCAGCTCGG AGTTTTGCGC - # - #
- # 20
- - - - (2) INFORMATION FOR SEQ ID NO: 78:
- - (i) SEQUENCE CHARACTERISTICS:
(A) LENGTH: 20
(B) TYPE: Nucleic Acid
(C) STRANDEDNESS: Single
(D) TOPOLOGY: Linear
- - (iv) ANTI-SENSE: Yes
- - (xi) SEQUENCE DESCRIPTION: SEQ ID NO: - # 78:
- - TTTTCTTCCA CTGCCCCTCA - # - #
- # 20
- - - - (2) INFORMATION FOR SEQ ID NO: 79:
- - (i) SEQUENCE CHARACTERISTICS:
(A) LENGTH: 20
(B) TYPE: Nucleic Acid
(C) STRANDEDNESS: Single
(D) TOPOLOGY: Linear
- - (iv) ANTI-SENSE: Yes
- - (xi) SEQUENCE DESCRIPTION: SEQ ID NO: - # 79:
- - CCCTTGGCTT CAGTACTCGG - # - #
- # 20
- - - - (2) INFORMATION FOR SEQ ID NO: 80:
- - (i) SEQUENCE CHARACTERISTICS:
(A) LENGTH: 20
(B) TYPE: Nucleic Acid
(C) STRANDEDNESS: Single
(D) TOPOLOGY: Linear
- - (iv) ANTI-SENSE: Yes
- - (xi) SEQUENCE DESCRIPTION: SEQ ID NO: - # 80:
- - CTTCCCACTC CAGCACATTG - # - #
- # 20
- - - - (2) INFORMATION FOR SEQ ID NO: 81:
- - (i) SEQUENCE CHARACTERISTICS:
(A) LENGTH: 20
(B) TYPE: Nucleic Acid
(C) STRANDEDNESS: Single
(D) TOPOLOGY: Linear
- - (iv) ANTI-SENSE: Yes
- - (xi) SEQUENCE DESCRIPTION: SEQ ID NO: - # 81:
- - GCACAGCCCG TTCGCAAAGC - # - #
- # 20
- - - - (2) INFORMATION FOR SEQ ID NO: 82:
- - (i) SEQUENCE CHARACTERISTICS:
(A) LENGTH: 20
(B) TYPE: Nucleic Acid
(C) STRANDEDNESS: Single
(D) TOPOLOGY: Linear
- - (iv) ANTI-SENSE: Yes
- - (xi) SEQUENCE DESCRIPTION: SEQ ID NO: - # 82:
- - AATGCAGCAG AGAGGTTGGG - # - #
- # 20
- - - - (2) INFORMATION FOR SEQ ID NO: 83:
- - (i) SEQUENCE CHARACTERISTICS:
(A) LENGTH: 20
(B) TYPE: Nucleic Acid
(C) STRANDEDNESS: Single
(D) TOPOLOGY: Linear
- - (iv) ANTI-SENSE: Yes
- - (xi) SEQUENCE DESCRIPTION: SEQ ID NO: - # 83:
- - GACGGGAGGG ACTACAGGCT - # - #
- # 20
- - - - (2) INFORMATION FOR SEQ ID NO: 84:
- - (i) SEQUENCE CHARACTERISTICS:
(A) LENGTH: 20
(B) TYPE: Nucleic Acid
(C) STRANDEDNESS: Single
(D) TOPOLOGY: Linear
- - (iv) ANTI-SENSE: Yes
- - (xi) SEQUENCE DESCRIPTION: SEQ ID NO: - # 84:
- - TCTGGACTTG TGGGTTGCTG - # - #
- # 20
- - - - (2) INFORMATION FOR SEQ ID NO: 85:
- - (i) SEQUENCE CHARACTERISTICS:
(A) LENGTH: 20
(B) TYPE: Nucleic Acid
(C) STRANDEDNESS: Single
(D) TOPOLOGY: Linear
- - (iv) ANTI-SENSE: Yes
- - (xi) SEQUENCE DESCRIPTION: SEQ ID NO: - # 85:
- - TAAACGATCA CAGCGCATGC - # - #
- # 20
- - - - (2) INFORMATION FOR SEQ ID NO: 86:
- - (i) SEQUENCE CHARACTERISTICS:
(A) LENGTH: 20
(B) TYPE: Nucleic Acid
(C) STRANDEDNESS: Single
(D) TOPOLOGY: Linear
- - (iv) ANTI-SENSE: Yes
- - (xi) SEQUENCE DESCRIPTION: SEQ ID NO: - # 86:
- - GGGAGGACGA GCAGCCAGTG - # - #
- # 20
- - - - (2) INFORMATION FOR SEQ ID NO: 87:
- - (i) SEQUENCE CHARACTERISTICS:
(A) LENGTH: 20
(B) TYPE: Nucleic Acid
(C) STRANDEDNESS: Single
(D) TOPOLOGY: Linear
- - (iv) ANTI-SENSE: Yes
- - (xi) SEQUENCE DESCRIPTION: SEQ ID NO: - # 87:
- - CCCGGCCTTT TGACCGCCTC - # - #
- # 20
- - - - (2) INFORMATION FOR SEQ ID NO: 88:
- - (i) SEQUENCE CHARACTERISTICS:
(A) LENGTH: 20
(B) TYPE: Nucleic Acid
(C) STRANDEDNESS: Single
(D) TOPOLOGY: Linear
- - (iv) ANTI-SENSE: Yes
- - (xi) SEQUENCE DESCRIPTION: SEQ ID NO: - # 88:
- - CCGCCTCCCC GGCCTTTTGA - # - #
- # 20
- - - - (2) INFORMATION FOR SEQ ID NO: 89:
- - (i) SEQUENCE CHARACTERISTICS:
(A) LENGTH: 20
(B) TYPE: Nucleic Acid
(C) STRANDEDNESS: Single
(D) TOPOLOGY: Linear
- - (iv) ANTI-SENSE: Yes
- - (xi) SEQUENCE DESCRIPTION: SEQ ID NO: - # 89:
- - CCGTCGTGGT CCTCCGTGAC - # - #
- # 20
- - - - (2) INFORMATION FOR SEQ ID NO: 90:
- - (i) SEQUENCE CHARACTERISTICS:
(A) LENGTH: 20
(B) TYPE: Nucleic Acid
(C) STRANDEDNESS: Single
(D) TOPOLOGY: Linear
- - (iv) ANTI-SENSE: Yes
- - (xi) SEQUENCE DESCRIPTION: SEQ ID NO: - # 90:
- - GTGACCGACG AGCAGGAGGG - # - #
- # 20
- - - - (2) INFORMATION FOR SEQ ID NO: 91:
- - (i) SEQUENCE CHARACTERISTICS:
(A) LENGTH: 20
(B) TYPE: Nucleic Acid
(C) STRANDEDNESS: Single
(D) TOPOLOGY: Linear
- - (iv) ANTI-SENSE: Yes
- - (xi) SEQUENCE DESCRIPTION: SEQ ID NO: - # 91:
- - AAAAGAAGGT GACGGGGAGT - # - #
- # 20
- - - - (2) INFORMATION FOR SEQ ID NO: 92:
- - (i) SEQUENCE CHARACTERISTICS:
(A) LENGTH: 20
(B) TYPE: Nucleic Acid
(C) STRANDEDNESS: Single
(D) TOPOLOGY: Linear
- - (iv) ANTI-SENSE: Yes
- - (xi) SEQUENCE DESCRIPTION: SEQ ID NO: - # 92:
- - TTCTCTTTTA GCCTCCCCCA - # - #
- # 20
- - - - (2) INFORMATION FOR SEQ ID NO: 93:
- - (i) SEQUENCE CHARACTERISTICS:
(A) LENGTH: 20
(B) TYPE: Nucleic Acid
(C) STRANDEDNESS: Single
(D) TOPOLOGY: Linear
- - (iv) ANTI-SENSE: Yes
- - (xi) SEQUENCE DESCRIPTION: SEQ ID NO: - # 93:
- - TCCCCCATTC TCTTTTAGCC - # - #
- # 20
- - - - (2) INFORMATION FOR SEQ ID NO: 94:
- - (i) SEQUENCE CHARACTERISTICS:
(A) LENGTH: 20
(B) TYPE: Nucleic Acid
(C) STRANDEDNESS: Single
(D) TOPOLOGY: Linear
- - (iv) ANTI-SENSE: Yes
- - (xi) SEQUENCE DESCRIPTION: SEQ ID NO: - # 94:
- - TTATCATCGA CAGCGCCACA - # - #
- # 20
- - - - (2) INFORMATION FOR SEQ ID NO: 95:
- - (i) SEQUENCE CHARACTERISTICS:
(A) LENGTH: 20
(B) TYPE: Nucleic Acid
(C) STRANDEDNESS: Single
(D) TOPOLOGY: Linear
- - (iv) ANTI-SENSE: Yes
- - (xi) SEQUENCE DESCRIPTION: SEQ ID NO: - # 95:
- - TGAGGGGCAG TGGAAGAAAA - # - #
- # 20
- - - - (2) INFORMATION FOR SEQ ID NO: 96:
- - (i) SEQUENCE CHARACTERISTICS:
(A) LENGTH: 20
(B) TYPE: Nucleic Acid
(C) STRANDEDNESS: Single
(D) TOPOLOGY: Linear
- - (iv) ANTI-SENSE: Yes
- - (xi) SEQUENCE DESCRIPTION: SEQ ID NO: - # 96:
- - GTTCTCGGCT CCGCCGGCTC - # - #
- # 20
- - - - (2) INFORMATION FOR SEQ ID NO: 97:
- - (i) SEQUENCE CHARACTERISTICS:
(A) LENGTH: 20
(B) TYPE: Nucleic Acid
(C) STRANDEDNESS: Single
(D) TOPOLOGY: Linear
- - (iv) ANTI-SENSE: Yes
- - (xi) SEQUENCE DESCRIPTION: SEQ ID NO: - # 97:
- - CATCATGGTC GTGGTTTGGG - # - #
- # 20
- - - - (2) INFORMATION FOR SEQ ID NO: 98:
- - (i) SEQUENCE CHARACTERISTICS:
(A) LENGTH: 20
(B) TYPE: Nucleic Acid
(C) STRANDEDNESS: Single
(D) TOPOLOGY: Linear
- - (iv) ANTI-SENSE: Yes
- - (xi) SEQUENCE DESCRIPTION: SEQ ID NO: - # 98:
- - TCCGCGTTGA AACCCGAGAA - # - #
- # 20
- - - - (2) INFORMATION FOR SEQ ID NO: 99:
- - (i) SEQUENCE CHARACTERISTICS:
(A) LENGTH: 20
(B) TYPE: Nucleic Acid
(C) STRANDEDNESS: Single
(D) TOPOLOGY: Linear
- - (iv) ANTI-SENSE: Yes
- - (xi) SEQUENCE DESCRIPTION: SEQ ID NO: - # 99:
- - TGGGCTGGTG GAGATGGCTG - # - #
- # 20
- - - - (2) INFORMATION FOR SEQ ID NO: 100:
- - (i) SEQUENCE CHARACTERISTICS:
(A) LENGTH: 20
(B) TYPE: Nucleic Acid
(C) STRANDEDNESS: Single
(D) TOPOLOGY: Linear
- - (iv) ANTI-SENSE: Yes
- - (xi) SEQUENCE DESCRIPTION: SEQ ID NO: - # 100:
- - CGATGCTCTG CGCTCTGCCG - # - #
- # 20
- - - - (2) INFORMATION FOR SEQ ID NO: 101:
- - (i) SEQUENCE CHARACTERISTICS:
(A) LENGTH: 20
(B) TYPE: Nucleic Acid
(C) STRANDEDNESS: Single
(D) TOPOLOGY: Linear
- - (iv) ANTI-SENSE: Yes
- - (xi) SEQUENCE DESCRIPTION: SEQ ID NO: - # 101:
- - TTCGGTGGGC AGCTGCGCAG - # - #
- # 20
- - - - (2) INFORMATION FOR SEQ ID NO: 102:
- - (i) SEQUENCE CHARACTERISTICS:
(A) LENGTH: 20
(B) TYPE: Nucleic Acid
(C) STRANDEDNESS: Single
(D) TOPOLOGY: Linear
- - (iv) ANTI-SENSE: Yes
- - (xi) SEQUENCE DESCRIPTION: SEQ ID NO: - # 102:
- - CAGGGCTAGC AGTGTGGGCG - # - #
- # 20
- - - - (2) INFORMATION FOR SEQ ID NO: 103:
- - (i) SEQUENCE CHARACTERISTICS:
(A) LENGTH: 20
(B) TYPE: Nucleic Acid
(C) STRANDEDNESS: Single
(D) TOPOLOGY: Linear
- - (iv) ANTI-SENSE: Yes
- - (xi) SEQUENCE DESCRIPTION: SEQ ID NO: - # 103:
- - CCAGCTCAGT CAGTGCCGGC - # - #
- # 20
- - - - (2) INFORMATION FOR SEQ ID NO: 104:
- - (i) SEQUENCE CHARACTERISTICS:
(A) LENGTH: 20
(B) TYPE: Nucleic Acid
(C) STRANDEDNESS: Single
(D) TOPOLOGY: Linear
- - (iv) ANTI-SENSE: Yes
- - (xi) SEQUENCE DESCRIPTION: SEQ ID NO: - # 104:
- - TCTACGGGAA CCCCTCGAGG - # - #
- # 20
- - - - (2) INFORMATION FOR SEQ ID NO: 105:
- - (i) SEQUENCE CHARACTERISTICS:
(A) LENGTH: 20
(B) TYPE: Nucleic Acid
(C) STRANDEDNESS: Single
(D) TOPOLOGY: Linear
- - (iv) ANTI-SENSE: Yes
- - (xi) SEQUENCE DESCRIPTION: SEQ ID NO: - # 105:
- - CTCCATGCGG TTGCTTTTGA - # - #
- # 20
- - - - (2) INFORMATION FOR SEQ ID NO: 106:
- - (i) SEQUENCE CHARACTERISTICS:
(A) LENGTH: 20
(B) TYPE: Nucleic Acid
(C) STRANDEDNESS: Single
(D) TOPOLOGY: Linear
- - (iv) ANTI-SENSE: Yes
- - (xi) SEQUENCE DESCRIPTION: SEQ ID NO: - # 106:
- - CAGGCCTGGC TCACATGCTA - # - #
- # 20
- - - - (2) INFORMATION FOR SEQ ID NO: 107:
- - (i) SEQUENCE CHARACTERISTICS:
(A) LENGTH: 20
(B) TYPE: Nucleic Acid
(C) STRANDEDNESS: Single
(D) TOPOLOGY: Linear
- - (iv) ANTI-SENSE: Yes
- - (xi) SEQUENCE DESCRIPTION: SEQ ID NO: - # 107:
- - AGATGCCCTT GGGGAGCTCC - # - #
- # 20
- - - - (2) INFORMATION FOR SEQ ID NO: 108:
- - (i) SEQUENCE CHARACTERISTICS:
(A) LENGTH: 20
(B) TYPE: Nucleic Acid
(C) STRANDEDNESS: Single
(D) TOPOLOGY: Linear
- - (iv) ANTI-SENSE: Yes
- - (xi) SEQUENCE DESCRIPTION: SEQ ID NO: - # 108:
- - TGACTATAGA CCGCCGCCGG - # - #
- # 20
- - - - (2) INFORMATION FOR SEQ ID NO: 109:
- - (i) SEQUENCE CHARACTERISTICS:
(A) LENGTH: 20
(B) TYPE: Nucleic Acid
(C) STRANDEDNESS: Single
(D) TOPOLOGY: Linear
- - (iv) ANTI-SENSE: Yes
- - (xi) SEQUENCE DESCRIPTION: SEQ ID NO: - # 109:
- - CCGCCGGTGA CTATAGACCG - # - #
- # 20
- - - - (2) INFORMATION FOR SEQ ID NO: 110:
- - (i) SEQUENCE CHARACTERISTICS:
(A) LENGTH: 20
(B) TYPE: Nucleic Acid
(C) STRANDEDNESS: Single
(D) TOPOLOGY: Linear
- - (iv) ANTI-SENSE: Yes
- - (xi) SEQUENCE DESCRIPTION: SEQ ID NO: - # 110:
- - TCAACCGGTA CGCCACGTGG - # - #
- # 20
- - - - (2) INFORMATION FOR SEQ ID NO: 111:
- - (i) SEQUENCE CHARACTERISTICS:
(A) LENGTH: 20
(B) TYPE: Nucleic Acid
(C) STRANDEDNESS: Single
(D) TOPOLOGY: Linear
- - (iv) ANTI-SENSE: Yes
- - (xi) SEQUENCE DESCRIPTION: SEQ ID NO: - # 111:
- - CCTCGAGGGG TTCCCGTAGA - # - #
- # 20
- - - - (2) INFORMATION FOR SEQ ID NO: 112:
- - (i) SEQUENCE CHARACTERISTICS:
(A) LENGTH: 20
(B) TYPE: Nucleic Acid
(C) STRANDEDNESS: Single
(D) TOPOLOGY: Linear
- - (iv) ANTI-SENSE: Yes
- - (xi) SEQUENCE DESCRIPTION: SEQ ID NO: - # 112:
- - GTCCGGACCG AGTGTACGAT - # - #
- # 20
- - - - (2) INFORMATION FOR SEQ ID NO: 113:
- - (i) SEQUENCE CHARACTERISTICS:
(A) LENGTH: 20
(B) TYPE: Nucleic Acid
(C) STRANDEDNESS: Single
(D) TOPOLOGY: Linear
- - (iv) ANTI-SENSE: Yes
- - (xi) SEQUENCE DESCRIPTION: SEQ ID NO: - # 113:
- - GCGCACCGTC ATTACGTCGA - # - #
- # 20
- - - - (2) INFORMATION FOR SEQ ID NO: 114:
- - (i) SEQUENCE CHARACTERISTICS:
(A) LENGTH: 20
(B) TYPE: Nucleic Acid
(C) STRANDEDNESS: Single
(D) TOPOLOGY: Linear
- - (iv) ANTI-SENSE: Yes
- - (xi) SEQUENCE DESCRIPTION: SEQ ID NO: - # 114:
- - ACGTCGAGCG CACCGTCATT - # - #
- # 20
- - - - (2) INFORMATION FOR SEQ ID NO: 115:
- - (i) SEQUENCE CHARACTERISTICS:
(A) LENGTH: 20
(B) TYPE: Nucleic Acid
(C) STRANDEDNESS: Single
(D) TOPOLOGY: Linear
- - (iv) ANTI-SENSE: Yes
- - (xi) SEQUENCE DESCRIPTION: SEQ ID NO: - # 115:
- - CACGCGTGCC TGACTTGGTA - # - #
- # 20
- - - - (2) INFORMATION FOR SEQ ID NO: 116:
- - (i) SEQUENCE CHARACTERISTICS:
(A) LENGTH: 20
(B) TYPE: Nucleic Acid
(C) STRANDEDNESS: Single
(D) TOPOLOGY: Linear
- - (iv) ANTI-SENSE: Yes
- - (xi) SEQUENCE DESCRIPTION: SEQ ID NO: - # 116:
- - TAGCATGTGA GCCAGGCCTG - # - #
- # 20
- - - - (2) INFORMATION FOR SEQ ID NO: 117:
- - (i) SEQUENCE CHARACTERISTICS:
(A) LENGTH: 20
(B) TYPE: Nucleic Acid
(C) STRANDEDNESS: Single
(D) TOPOLOGY: Linear
- - (iv) ANTI-SENSE: Yes
- - (xi) SEQUENCE DESCRIPTION: SEQ ID NO: - # 117:
- - TTCTCACCCA CCACGTACGT - # - #
- # 20
- - - - (2) INFORMATION FOR SEQ ID NO: 118:
- - (i) SEQUENCE CHARACTERISTICS:
(A) LENGTH: 16
(B) TYPE: Nucleic Acid
(C) STRANDEDNESS: Single
(D) TOPOLOGY: Linear
- - (iv) ANTI-SENSE: Yes
- - (xi) SEQUENCE DESCRIPTION: SEQ ID NO: - # 118:
- - TGCGGGTGAG TGGTAG - # - #
- # 16
- - - - (2) INFORMATION FOR SEQ ID NO: 119:
- - (i) SEQUENCE CHARACTERISTICS:
(A) LENGTH: 20
(B) TYPE: Nucleic Acid
(C) STRANDEDNESS: Single
(D) TOPOLOGY: Linear
- - (iv) ANTI-SENSE: Yes
- - (xi) SEQUENCE DESCRIPTION: SEQ ID NO: - # 119:
- - GCCGCGGGAC CAGCCCCAGC - # - #
- # 20
- - - - (2) INFORMATION FOR SEQ ID NO: 120:
- - (i) SEQUENCE CHARACTERISTICS:
(A) LENGTH: 16
(B) TYPE: Nucleic Acid
(C) STRANDEDNESS: Single
(D) TOPOLOGY: Linear
- - (iv) ANTI-SENSE: Yes
- - (xi) SEQUENCE DESCRIPTION: SEQ ID NO: - # 120:
- - TGCGGGTGAG TGGTAG - # - #
- # 16
- - - - (2) INFORMATION FOR SEQ ID NO: 121:
- - (i) SEQUENCE CHARACTERISTICS:
(A) LENGTH: 16
(B) TYPE: Nucleic Acid
(C) STRANDEDNESS: Single
(D) TOPOLOGY: Linear
- - (iv) ANTI-SENSE: Yes
- - (xi) SEQUENCE DESCRIPTION: SEQ ID NO: - # 121:
- - CGCTGCAGAT GCGGTT - # - #
- # 16
- - - - (2) INFORMATION FOR SEQ ID NO: 122:
- - (i) SEQUENCE CHARACTERISTICS:
(A) LENGTH: 16
(B) TYPE: Nucleic Acid
(C) STRANDEDNESS: Single
(D) TOPOLOGY: Linear
- - (iv) ANTI-SENSE: Yes
- - (xi) SEQUENCE DESCRIPTION: SEQ ID NO: - # 122:
- - CCGCCGGCTC AGTCTT - # - #
- # 16
- - - - (2) INFORMATION FOR SEQ ID NO: 123:
- - (i) SEQUENCE CHARACTERISTICS:
(A) LENGTH: 16
(B) TYPE: Nucleic Acid
(C) STRANDEDNESS: Single
(D) TOPOLOGY: Linear
- - (iv) ANTI-SENSE: Yes
- - (xi) SEQUENCE DESCRIPTION: SEQ ID NO: - # 123:
- - CATCGTGGCG GTTAGG - # - #
- # 16
- - - - (2) INFORMATION FOR SEQ ID NO: 124:
- - (i) SEQUENCE CHARACTERISTICS:
(A) LENGTH: 30
(B) TYPE: Nucleic Acid
(C) STRANDEDNESS: Single
(D) TOPOLOGY: Linear
- - (iv) ANTI-SENSE: Yes
- - (xi) SEQUENCE DESCRIPTION: SEQ ID NO: - # 124:
- - CCATCTTAAT AAATAAATTA AAAACACAAT - # - #
30
- - - - (2) INFORMATION FOR SEQ ID NO: 125:
- - (i) SEQUENCE CHARACTERISTICS:
(A) LENGTH: 20
(B) TYPE: Nucleic Acid
(C) STRANDEDNESS: Single
(D) TOPOLOGY: Linear
- - (iv) ANTI-SENSE: Yes
- - (xi) SEQUENCE DESCRIPTION: SEQ ID NO: - # 125:
- - AAATAAATTA AAAACACAAT - # - #
- # 20
- - - - (2) INFORMATION FOR SEQ ID NO: 126:
- - (i) SEQUENCE CHARACTERISTICS:
(A) LENGTH: 20
(B) TYPE: Nucleic Acid
(C) STRANDEDNESS: Single
(D) TOPOLOGY: Linear
- - (iv) ANTI-SENSE: Yes
- - (xi) SEQUENCE DESCRIPTION: SEQ ID NO: - # 126:
- - AATTAAAAAC ACAATAAAAC - # - #
- # 20
- - - - (2) INFORMATION FOR SEQ ID NO: 127:
- - (i) SEQUENCE CHARACTERISTICS:
(A) LENGTH: 20
(B) TYPE: Nucleic Acid
(C) STRANDEDNESS: Single
(D) TOPOLOGY: Linear
- - (iv) ANTI-SENSE: Yes
- - (xi) SEQUENCE DESCRIPTION: SEQ ID NO: - # 127:
- - ATATAAATAT CTGAGAATCC - # - #
- # 20
- - - - (2) INFORMATION FOR SEQ ID NO: 128:
- - (i) SEQUENCE CHARACTERISTICS:
(A) LENGTH: 20
(B) TYPE: Nucleic Acid
(C) STRANDEDNESS: Single
(D) TOPOLOGY: Linear
- - (iv) ANTI-SENSE: Yes
- - (xi) SEQUENCE DESCRIPTION: SEQ ID NO: - # 128:
- - ATCTGAGAAT CCATCTTAAT - # - #
- # 20
- - - - (2) INFORMATION FOR SEQ ID NO: 129:
- - (i) SEQUENCE CHARACTERISTICS:
(A) LENGTH: 20
(B) TYPE: Nucleic Acid
(C) STRANDEDNESS: Single
(D) TOPOLOGY: Linear
- - (iv) ANTI-SENSE: Yes
- - (xi) SEQUENCE DESCRIPTION: SEQ ID NO: - # 129:
- - AAATATAAAT ATCTGAGAAT - # - #
- # 20
- - - - (2) INFORMATION FOR SEQ ID NO: 130:
- - (i) SEQUENCE CHARACTERISTICS:
(A) LENGTH: 20
(B) TYPE: Nucleic Acid
(C) STRANDEDNESS: Single
(D) TOPOLOGY: Linear
- - (iv) ANTI-SENSE: Yes
- - (xi) SEQUENCE DESCRIPTION: SEQ ID NO: - # 130:
- - AAGACCTCAA GGTAGAAAAA - # - #
- # 20
- - - - (2) INFORMATION FOR SEQ ID NO: 131:
- - (i) SEQUENCE CHARACTERISTICS:
(A) LENGTH: 30
(B) TYPE: Nucleic Acid
(C) STRANDEDNESS: Single
(D) TOPOLOGY: Linear
- - (iv) ANTI-SENSE: Yes
- - (xi) SEQUENCE DESCRIPTION: SEQ ID NO: - # 131:
- - CCATCTTAAT AAATAAATTA AAAACACAAT - # - #
30
- - - - (2) INFORMATION FOR SEQ ID NO: 132:
- - (i) SEQUENCE CHARACTERISTICS:
(A) LENGTH: 20
(B) TYPE: Nucleic Acid
(C) STRANDEDNESS: Single
(D) TOPOLOGY: Linear
- - (iv) ANTI-SENSE: Yes
- - (xi) SEQUENCE DESCRIPTION: SEQ ID NO: - # 132:
- - AAATAAATTA AAAACACAAT - # - #
- # 20
- - - - (2) INFORMATION FOR SEQ ID NO: 133:
- - (i) SEQUENCE CHARACTERISTICS:
(A) LENGTH: 20
(B) TYPE: Nucleic Acid
(C) STRANDEDNESS: Single
(D) TOPOLOGY: Linear
- - (iv) ANTI-SENSE: Yes
- - (xi) SEQUENCE DESCRIPTION: SEQ ID NO: - # 133:
- - AATTAAAAAC ACAATAAAAC - # - #
- # 20
- - - - (2) INFORMATION FOR SEQ ID NO: 134:
- - (i) SEQUENCE CHARACTERISTICS:
(A) LENGTH: 20
(B) TYPE: Nucleic Acid
(C) STRANDEDNESS: Single
(D) TOPOLOGY: Linear
- - (iv) ANTI-SENSE: Yes
- - (xi) SEQUENCE DESCRIPTION: SEQ ID NO: - # 134:
- - ATATAAATAT CTGAGAATCC - # - #
- # 20
- - - - (2) INFORMATION FOR SEQ ID NO: 135:
- - (i) SEQUENCE CHARACTERISTICS:
(A) LENGTH: 20
(B) TYPE: Nucleic Acid
(C) STRANDEDNESS: Single
(D) TOPOLOGY: Linear
- - (iv) ANTI-SENSE: Yes
- - (xi) SEQUENCE DESCRIPTION: SEQ ID NO: - # 135:
- - ATATAAATAT CTGAGAATCC - # - #
- # 20
- - - - (2) INFORMATION FOR SEQ ID NO: 136:
- - (i) SEQUENCE CHARACTERISTICS:
(A) LENGTH: 20
(B) TYPE: Nucleic Acid
(C) STRANDEDNESS: Single
(D) TOPOLOGY: Linear
- - (iv) ANTI-SENSE: Yes
- - (xi) SEQUENCE DESCRIPTION: SEQ ID NO: - # 136:
- - ATCTGAGAAT CCATCTTAAT - # - #
- # 20
- - - - (2) INFORMATION FOR SEQ ID NO: 137:
- - (i) SEQUENCE CHARACTERISTICS:
(A) LENGTH: 20
(B) TYPE: Nucleic Acid
(C) STRANDEDNESS: Single
(D) TOPOLOGY: Linear
- - (iv) ANTI-SENSE: Yes
- - (xi) SEQUENCE DESCRIPTION: SEQ ID NO: - # 137:
- - AAATATAAAT ATCTGAGAAT - # - #
- # 20
- - - - (2) INFORMATION FOR SEQ ID NO: 138:
- - (i) SEQUENCE CHARACTERISTICS:
(A) LENGTH: 20
(B) TYPE: Nucleic Acid
(C) STRANDEDNESS: Single
(D) TOPOLOGY: Linear
- - (iv) ANTI-SENSE: Yes
- - (xi) SEQUENCE DESCRIPTION: SEQ ID NO: - # 138:
- - AAGACCTCAA GGTAGAAAAA - # - #
- # 20
- - - - (2) INFORMATION FOR SEQ ID NO: 139:
- - (i) SEQUENCE CHARACTERISTICS:
(A) LENGTH: 29
(B) TYPE: Nucleic Acid
(C) STRANDEDNESS: Single
(D) TOPOLOGY: Linear
- - (iv) ANTI-SENSE: No
- - (xi) SEQUENCE DESCRIPTION: SEQ ID NO: - # 139:
- - ACGGGGAGTC GGGGCTGCCA GAGAGAAGT - # - #
29
__________________________________________________________________________
Claims (44)
5'- TGCCCCTCAGCCCCCGACGC SEQ ID NO: 9,
- 5'- TCAGCCCCCGACGGTCTCTC -3' SEQ ID
NO: 8,
- or
- 5'- CCCCCGACGGTCTCTCTTCA-3' SEQ ID NO: 7.
Priority Applications (8)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US08/837,201 US5985558A (en) | 1997-04-14 | 1997-04-14 | Antisense oligonucleotide compositions and methods for the inibition of c-Jun and c-Fos |
| EP98915526A EP0975371A4 (en) | 1997-04-14 | 1998-04-14 | ANTISENSE OLIGONUCLEOTID COMPOSITIONS AND METHODS OF MODULATING ACTIVATION PROTEIN 1 |
| PCT/US1998/007386 WO1998046272A1 (en) | 1997-04-14 | 1998-04-14 | Antisense oligonucleotide compositions and methods for the modulation of activating protein 1 |
| AU69688/98A AU6968898A (en) | 1997-04-14 | 1998-04-14 | Antisense oligonucleotide compositions and methods for the modulation of activating protein |
| US09/364,416 US6312900B1 (en) | 1997-04-14 | 1999-07-30 | Antisense oligonucleotide compositions and methods for the modulation of activating protein 1 |
| US09/923,517 US20020039741A1 (en) | 1997-04-14 | 2001-08-07 | Antisense oligonucleotide compositions and methods for the modulation of activating protein 1 |
| US10/430,196 US20030194738A1 (en) | 1997-04-14 | 2003-05-05 | Antisense oligonucleotide compositions and methods for the modulation of activating protein 1 |
| US11/072,846 US20060154885A1 (en) | 1992-10-05 | 2005-03-04 | Modulation of SLC26A2 expression |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US08/837,201 US5985558A (en) | 1997-04-14 | 1997-04-14 | Antisense oligonucleotide compositions and methods for the inibition of c-Jun and c-Fos |
Related Child Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US09/364,416 Continuation US6312900B1 (en) | 1992-10-05 | 1999-07-30 | Antisense oligonucleotide compositions and methods for the modulation of activating protein 1 |
Publications (1)
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| US5985558A true US5985558A (en) | 1999-11-16 |
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ID=25273801
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| US08/837,201 Expired - Lifetime US5985558A (en) | 1992-10-05 | 1997-04-14 | Antisense oligonucleotide compositions and methods for the inibition of c-Jun and c-Fos |
| US09/364,416 Expired - Lifetime US6312900B1 (en) | 1992-10-05 | 1999-07-30 | Antisense oligonucleotide compositions and methods for the modulation of activating protein 1 |
| US09/923,517 Abandoned US20020039741A1 (en) | 1992-10-05 | 2001-08-07 | Antisense oligonucleotide compositions and methods for the modulation of activating protein 1 |
| US10/430,196 Abandoned US20030194738A1 (en) | 1992-10-05 | 2003-05-05 | Antisense oligonucleotide compositions and methods for the modulation of activating protein 1 |
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| US09/364,416 Expired - Lifetime US6312900B1 (en) | 1992-10-05 | 1999-07-30 | Antisense oligonucleotide compositions and methods for the modulation of activating protein 1 |
| US09/923,517 Abandoned US20020039741A1 (en) | 1992-10-05 | 2001-08-07 | Antisense oligonucleotide compositions and methods for the modulation of activating protein 1 |
| US10/430,196 Abandoned US20030194738A1 (en) | 1992-10-05 | 2003-05-05 | Antisense oligonucleotide compositions and methods for the modulation of activating protein 1 |
Country Status (4)
| Country | Link |
|---|---|
| US (4) | US5985558A (en) |
| EP (1) | EP0975371A4 (en) |
| AU (1) | AU6968898A (en) |
| WO (1) | WO1998046272A1 (en) |
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| US20030194738A1 (en) | 2003-10-16 |
| US20020039741A1 (en) | 2002-04-04 |
| EP0975371A4 (en) | 2002-10-23 |
| EP0975371A1 (en) | 2000-02-02 |
| US6312900B1 (en) | 2001-11-06 |
| WO1998046272A1 (en) | 1998-10-22 |
| AU6968898A (en) | 1998-11-11 |
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